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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCB11
(R832C)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
ABCB4
Deletion
(splice donor variant)
Progressive familial intrahepatic cholestasis type 3
GLikely pathogenic
ABCB4
(R969H)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
ABCB4
(E898K)
Single nucleotide variant
(missense variant)
Progressive familial intrahepatic cholestasis type 3
GPathogenic/Likely pathogenic
ABCB4
(T775M)
Single nucleotide variant
(missense variant)
Cholestasis, intrahepatic, of pregnancy, 3
+3 more
GConflicting classifications of pathogenicity
ABCB4
(N510S)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
ABCB4
(R406*)
Single nucleotide variant
(nonsense)
Progressive familial intrahepatic cholestasis type 3
+1 more
GPathogenic
ABCB4
(G384V)
Single nucleotide variant
(missense variant)
Progressive familial intrahepatic cholestasis type 3
+2 more
GUncertain significance
ABCB4
Single nucleotide variant
(synonymous variant)
Progressive familial intrahepatic cholestasis type 3
GUncertain significance
ABCB4
(L260P)
Single nucleotide variant
(missense variant)
Cholestasis, intrahepatic, of pregnancy, 3
+2 more
GUncertain significance
ABCB4
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ABCB4
(R176W)
Single nucleotide variant
(missense variant)
Progressive familial intrahepatic cholestasis type 3
+3 more
GPathogenic/Likely pathogenic
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