C4016270[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 181178	NM_000257.4(MYH7):c.2229G>C (p.Glu743Asp)	MYH7 (E743D)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +1 more	GUncertain significance
Select item 4243	NM_033118.4(MYLK2):c.260C>T (p.Ala87Val)	MYLK2 (A87V)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 4244	NM_033118.4(MYLK2):c.284C>A (p.Ala95Glu)	MYLK2 (A95E)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign

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