ClinVar Miner

List of variants in gene EMD reported as benign for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000117.3(EMD):c.465C>T (p.Tyr155=)	rs143447675	0.00375
NM_000117.3(EMD):c.445G>C (p.Asp149His)	rs2070818	0.00019

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