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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN5A
(M1700I +5 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+1 more
GUncertain significance
NEDD4L
(R425C +6 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
LOC130064563, GSK3A
(G49A)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GUncertain significance
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