"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC114827 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14065	NM_000432.4(MYL2):c.64G>A (p.Glu22Lys)	LOC114827850, MYL2 (E22K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GPathogenic/Likely pathogenic
Select item 43474	NM_000432.4(MYL2):c.4-14C>T	LOC114827850, MYL2	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 307216	NM_000432.4(MYL2):c.3+9A>G	LOC114827850, MYL2	Single nucleotide variant (intron variant)	MYL2-related disorder +2 more	GConflicting classifications of pathogenicity

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ClinVar