ClinVar for PubMed (Select 26116789) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2701264	NM_000432.4(MYL2):c.172C>G (p.Arg58Gly)	MYL2 (R58G +2 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 10	GUncertain significance
Select item 31766	NM_000432.4(MYL2):c.141C>A (p.Asn47Lys)	MYL2 (N47K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 14067	NM_000432.4(MYL2):c.173G>A (p.Arg58Gln)	MYL2 (R58Q)	Single nucleotide variant (missense variant)	not provided +4 more	GPathogenic

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