ClinVar Miner

List of variants in gene combination LOC126861898, MYH7 reported as likely benign for Myosin storage myopathy

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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_000257.4(MYH7):c.2349C>T (p.Arg783=)	rs139882431	0.00036
NM_000257.4(MYH7):c.2360G>A (p.Arg787His)	rs376754645	0.00006

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