ClinVar Miner

List of variants in gene LOC126861898, MYH7 studied for Myopathy, myosin storage, autosomal recessive; Myosin storage myopathy; Dilated cardiomyopathy 1S; MYH7-related skeletal myopathy

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.2585C>T (p.Ala862Val)	rs149576470	0.00004

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