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Links from Gene

Items: 70

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BDNF, BDNF-AS
(E110* +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
(N109S +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
(G134S +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant +2 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant +2 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant +2 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
BDNF-related disorder
GLikely benign
BDNF-AS, BDNF
Single nucleotide variant
(synonymous variant +2 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
(V66M +4 more)
Single nucleotide variant
(non-coding transcript variant +3 more)
Post-traumatic stress disorder
GLikely risk allele
BDNF, BDNF-AS
(S140P +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
BDNF, BDNF-AS
(W212fs +4 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
+1 more
GLikely benign
BDNF, BDNF-AS
(I231V +4 more)
Single nucleotide variant
(missense variant)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(V128M +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GUncertain significance
BDNF, BDNF-AS
(N71K)
Single nucleotide variant
(missense variant +2 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(I68M)
Single nucleotide variant
(missense variant +2 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(G113D +4 more)
Single nucleotide variant
(missense variant)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(R120Q +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(L16fs)
Duplication
(frameshift variant +2 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(V56A)
Single nucleotide variant
(missense variant +2 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(F73L)
Single nucleotide variant
(missense variant +2 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(T10N +4 more)
Single nucleotide variant
(missense variant)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(M220T +4 more)
Single nucleotide variant
(missense variant)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(M122T +4 more)
Single nucleotide variant
(missense variant)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(K105E +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
GUncertain significance
BDNF, BDNF-AS
(Q157E +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
BDNF, BDNF-AS
(A106T +4 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
BDNF, BDNF-AS
(T77A +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
BDNF, BDNF-AS
(T86K +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
BDNF, BDNF-AS
(L125P +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
BDNF, BDNF-AS
(R93Q +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
BDNF, BDNF-AS
(G55V +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
BDNF, BDNF-AS
(K17E +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BDNF, BDNF-AS
(M130I +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
BDNF, BDNF-AS
(F116Y +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
BDNF-related disorder
+1 more
GLikely benign
BDNF, BDNF-AS
(C34fs)
Deletion
(frameshift variant +2 more)
BDNF-related disorder
GLikely benign
BDNF, BDNF-AS
(V215M +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(intron variant)
not provided
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(intron variant)
not provided
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
BDNF, BDNF-AS
(L16P)
Single nucleotide variant
(missense variant +2 more)
not specified
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(intron variant)
not provided
GBenign
BDNF, BDNF-AS
Microsatellite
(5 prime UTR variant +1 more)
not provided
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
BDNF-AS, BDNF
Single nucleotide variant
(intron variant)
not provided
GBenign
BDNF, BDNF-AS
Microsatellite
(5 prime UTR variant +1 more)
not provided
GBenign
BDNF, BDNF-AS
(C186Y +4 more)
Single nucleotide variant
(missense variant)
Obesity
GLikely pathogenic
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
BDNF-related disorder
+1 more
GLikely benign
BDNF, BDNF-AS
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
GBenign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
BDNF, BDNF-AS
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
BDNF, BDNF-AS
(E23K)
Single nucleotide variant
(missense variant +2 more)
Obesity
GBenign
BDNF, BDNF-AS
(E168* +4 more)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
GLikely pathogenic
BDNF, BDNF-AS
(S6fs)
Deletion
(frameshift variant +2 more)
not specified
GUncertain significance
BDNF, BDNF-AS
Single nucleotide variant
(no sequence alteration)
not specified
+1 more
GBenign
BDNF, BDNF-AS
(V66M +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GBenign
BDNF, BDNF-AS
(T2I +4 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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