List of variants reported as uncertain significance for Thomsen and Becker disease by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000083.3(CLCN1):c.2219C>G (p.Ser740Cys)	rs139262486	0.00031
NM_000083.3(CLCN1):c.2722A>G (p.Asn908Asp)	rs146862992	0.00015
NM_000083.3(CLCN1):c.652G>A (p.Ala218Thr)	rs189963844	0.00008
NM_000083.3(CLCN1):c.898C>T (p.Arg300Trp)	rs368280521	0.00002

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