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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861013, ABCC2
(R1100C)
Single nucleotide variant
(missense variant)
Dubin-Johnson syndrome
+1 more
GUncertain significance
ABCC2, LOC126861013
(R1100H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCC2, LOC126861013
(T1112N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCC2, LOC126861013
(I1126del)
Microsatellite
(inframe_deletion)
not provided
GUncertain significance
ABCC2, LOC126861013
(V1127I)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
ABCC2, LOC126861013
(Y1134fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
ABCC2, LOC126861013
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
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