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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC2, LOC108281165
(K57R)
Single nucleotide variant
(missense variant)
Dubin-Johnson syndrome
GUncertain significance
ABCC2
(G758V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ABCC2
(L834P)
Single nucleotide variant
(missense variant)
Dubin-Johnson syndrome
GUncertain significance
ABCC2
(I1173F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
ABCC2
(G1325S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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