List of variants reported as not provided for Thomsen and Becker disease

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000083.3(CLCN1):c.501C>G (p.Phe167Leu)	rs149729531	0.00075
NM_000083.3(CLCN1):c.1453A>G (p.Met485Val)	rs146457619	0.00039
NM_000083.3(CLCN1):c.2258A>C (p.Gln753Pro)	rs112282456	0.00010
NM_000083.3(CLCN1):c.2693G>A (p.Gly898Glu)	rs149188892	0.00005
NM_000083.3(CLCN1):c.1781G>T (p.Gly594Val)	rs746346988	0.00002
NM_000083.3(CLCN1):c.517C>T (p.Leu173Phe)	rs1554434802	0.00002
NM_000083.3(CLCN1):c.1863A>G (p.Thr621=)	rs369099862	0.00001
NM_000083.3(CLCN1):c.950G>A (p.Arg317Gln)	rs80356702	0.00001
NM_000083.3(CLCN1):c.1437_1450del (p.Pro480fs)	rs768119034
NM_000083.3(CLCN1):c.689G>A (p.Gly230Glu)	rs80356700

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