List of variants reported as uncertain significance for hereditary skeletal muscle disorder by Institute of Immunology and Genetics Kaiserslautern

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.1916A>G (p.Tyr639Cys)	rs747459771	0.00001
NM_000069.3(CACNA1S):c.4685T>C (p.Ile1562Thr)
NM_000334.4(SCN4A):c.4243G>A (p.Gly1415Ser)
NM_001100.4(ACTA1):c.954G>C (p.Glu318Asp)
NM_001267550.2(TTN):c.99865+2T>C

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