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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA4-AS1, LAMA4
(D35E)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1JJ
+2 more
GUncertain significance
LOC126861896, MYH6
(S1598L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 14
+4 more
GUncertain significance
MYLK2
(M474V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
GUncertain significance
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