List of variants reported as uncertain significance for malignant hyperthermia, susceptibility to, 1 by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.10422C>G (p.Asn3474Lys)	rs769661588	0.00002
NM_000540.3(RYR1):c.9971T>C (p.Val3324Ala)	rs141515745	0.00002
NM_000540.3(RYR1):c.13370T>G (p.Met4457Arg)	rs1394722307	0.00001
NM_000540.3(RYR1):c.4744G>A (p.Glu1582Lys)	rs1200734670	0.00001
NM_000540.3(RYR1):c.6139G>C (p.Asp2047His)	rs763963516	0.00001
NM_000540.3(RYR1):c.9559C>T (p.Arg3187Trp)	rs1376794459	0.00001
NM_000540.3(RYR1):c.10477C>T (p.Arg3493Cys)	rs750367227
NM_000540.3(RYR1):c.12024G>C (p.Gln4008His)	rs1972429144
NM_000540.3(RYR1):c.1291G>A (p.Ala431Thr)	rs768357333
NM_000540.3(RYR1):c.1440+2T>G	rs1555767403
NM_000540.3(RYR1):c.14647-3_14647del	rs1568611362
NM_000540.3(RYR1):c.3526A>G (p.Thr1176Ala)	rs1968278835
NM_000540.3(RYR1):c.5318C>G (p.Pro1773Arg)	rs1969269453

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