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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSD3B7
(E167*)
Single nucleotide variant
(nonsense)
Congenital bile acid synthesis defect 1
+1 more
GPathogenic
HSD3B7
(T186M)
Single nucleotide variant
(missense variant +1 more)
Congenital bile acid synthesis defect 1
GUncertain significance
HSD3B7
(R190H)
Single nucleotide variant
(missense variant +1 more)
Congenital bile acid synthesis defect 1
GUncertain significance
HSD3B7
(T323M)
Single nucleotide variant
(3 prime UTR variant +1 more)
Congenital bile acid synthesis defect 1
GUncertain significance
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