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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCB11
(R698H)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
ABCB11
Single nucleotide variant
(intron variant)
Benign recurrent intrahepatic cholestasis type 2
+4 more
GPathogenic/Likely pathogenic
ABCB11
(E592Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ABCB11
(R487H)
Single nucleotide variant
(missense variant)
Progressive familial intrahepatic cholestasis type 2
+4 more
GPathogenic/Likely pathogenic
ABCB4
(E1099G +2 more)
Single nucleotide variant
(missense variant)
Cholestasis, intrahepatic, of pregnancy, 3
+3 more
GUncertain significance
ABCB4
(P726L)
Single nucleotide variant
(missense variant)
Low phospholipid associated cholelithiasis
+3 more
GConflicting classifications of pathogenicity
ABCB4
(L73V)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
ABCB4
(T34M)
Single nucleotide variant
(missense variant)
Low phospholipid associated cholelithiasis
+4 more
GConflicting classifications of pathogenicity
ABCB4, LOC129998757
Single nucleotide variant
(5 prime UTR variant)
Cholestasis, intrahepatic, of pregnancy, 3
+2 more
GUncertain significance
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