List of variants reported as uncertain significance for Congenital myopathy by CSER _CC_NCGL, University of Washington

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.4405C>T (p.Arg1469Trp)	rs200546266	0.00010
NM_000540.3(RYR1):c.2956C>T (p.Arg986Cys)	rs150993059	0.00006
NM_000540.3(RYR1):c.9758T>C (p.Ile3253Thr)	rs375626634	0.00006
NM_000540.3(RYR1):c.14468C>T (p.Thr4823Met)	rs148540135	0.00004

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