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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC9
(H730Q +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
ABCC9
(R663C +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+7 more
GConflicting classifications of pathogenicity
ABCC9
(E629D +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
ABCC9
(R620Q +1 more)
Single nucleotide variant
(missense variant)
Primary familial dilated cardiomyopathy
+3 more
GUncertain significance
ABCC9
(V113I)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1O
+2 more
GUncertain significance
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