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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC9
(R1546L +1 more)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
GUncertain significance
ABCC9
(L1524fs)
Indel
(frameshift variant +1 more)
not provided
+5 more
GUncertain significance
ABCC9
(V1451A +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
ABCC9
(R1386H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ABCC9
(R1095H +1 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
ABCC9
(L662P +1 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
ABCC9
(V637I +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ABCC9
(F628fs +1 more)
Deletion
(frameshift variant)
Arrhythmogenic right ventricular cardiomyopathy
GUncertain significance
ABCC9
(S53fs)
Deletion
(frameshift variant +1 more)
not provided
GUncertain significance
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