ClinVar Miner

List of variants in gene combination LOC126861897, MHRT, MYH7 reported by Laboratory of Genetics and Molecular Cardiology, University of São Paulo

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His)	rs373514686	0.00001
NM_000257.4(MYH7):c.4992C>A (p.Asn1664Lys)	rs763538103

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