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Items: 1 to 100 of 527

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NCF2
Deletion
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
Deletion
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
Deletion
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
Deletion
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
Deletion
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
(A97D)
Single nucleotide variant
(missense variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely pathogenic
NCF2
Microsatellite
(frameshift variant +2 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely pathogenic
NCF2
Single nucleotide variant
(splice acceptor variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely pathogenic
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
NCF2-related disorder
+1 more
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
(R350W +3 more)
Indel
(missense variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
(Y394D +3 more)
Single nucleotide variant
(missense variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely pathogenic
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
(V445L +3 more)
Single nucleotide variant
(missense variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GUncertain significance
NCF2
(E235K +3 more)
Single nucleotide variant
(missense variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GBenign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Deletion
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(splice acceptor variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GUncertain significance
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
(Y82*)
Single nucleotide variant
(nonsense)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(splice acceptor variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely pathogenic
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
(C210* +3 more)
Single nucleotide variant
(nonsense)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GPathogenic
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Duplication
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant +1 more)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(synonymous variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
NCF2
Single nucleotide variant
(intron variant)
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
GLikely benign
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