ClinVar Miner

List of variants reported as uncertain significance for Myosin storage myopathy by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.2335G>A (p.Glu779Lys)	rs1427104281
NM_000257.4(MYH7):c.2869C>A (p.Leu957Met)
NM_000257.4(MYH7):c.3721G>T (p.Ala1241Ser)	rs757538583

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