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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRKAG2
(R302Q +4 more)
Single nucleotide variant
(missense variant)
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
+8 more
GPathogenic
LOC126861898, MYH7
(A797T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+18 more
GPathogenic/Likely pathogenic