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Links from Gene

Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126862416, HSD17B2
(M189T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSD17B2, LOC126862416
(S218R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSD17B2, LOC126862416
(V199A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSD17B2
Copy number loss
not provided
GUncertain significance
HSD17B2, LOC126862416
(L204F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSD17B2, LOC126862416
(T175S)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
HSD17B2, LOC126862416
(L179F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSD17B2, LOC126862416
(P174L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HSD17B2, LOC126862416
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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