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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861898, MYH7
(L881P)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+1 more
GConflicting classifications of pathogenicity
LOC126861898, MYH7
(K865R)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
LOC126861898, MYH7
(A797T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+18 more
GPathogenic/Likely pathogenic
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