List of variants reported as risk factor for Malignant hyperthermia, susceptibility to, 1 by OMIM

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.1840C>T (p.Arg614Cys)	rs118192172	0.00011
NM_000540.3(RYR1):c.7300G>A (p.Gly2434Arg)	rs121918593	0.00006
NM_000540.3(RYR1):c.6617C>T (p.Thr2206Met)	rs118192177	0.00004
NM_000540.3(RYR1):c.6487C>T (p.Arg2163Cys)	rs118192175	0.00001
NM_000540.3(RYR1):c.7372C>T (p.Arg2458Cys)	rs28933397	0.00001
NM_000540.3(RYR1):c.7373G>A (p.Arg2458His)	rs121918594	0.00001
NM_000540.2(RYR1):c.[8026C>T;8360C>G]
NM_000540.3(RYR1):c.1021G>A (p.Gly341Arg)	rs121918592
NM_000540.3(RYR1):c.14477C>T (p.Thr4826Ile)	rs121918595
NM_000540.3(RYR1):c.1565A>C (p.Tyr522Ser)	rs118192162
NM_000540.3(RYR1):c.487C>T (p.Arg163Cys)	rs118192161
NM_000540.3(RYR1):c.6488G>A (p.Arg2163His)	rs118192163
NM_000540.3(RYR1):c.6502G>A (p.Val2168Met)	rs118192176
NM_000540.3(RYR1):c.7039GAG[1] (p.Glu2348del)	rs121918596
NM_000540.3(RYR1):c.742G>A (p.Gly248Arg)	rs1801086

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