"Center for Genomic Medicine, King Faisal Specialist Hospital and Rese - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 802893	NM_000432.4(MYL2):c.3+2T>C	LOC114827850, MYL2	Single nucleotide variant (intron variant +1 more)	Hypertrophic cardiomyopathy 10 +1 more	GConflicting classifications of pathogenicity
Select item 3065627	NM_000432.4(MYL2):c.3+1G>A	LOC114827850, MYL2	Single nucleotide variant (intron variant +1 more)	Hypertrophic cardiomyopathy 10 +1 more	GConflicting classifications of pathogenicity