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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOM1
(Y1222C +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
MYOM1
(G1140E +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
MYOM1
(L390F)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
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