List of variants reported as likely benign for myosclerosis by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001849.4(COL6A2):c.2160C>G (p.Arg720=)	rs61735829	0.01898
NM_001849.4(COL6A2):c.316G>A (p.Glu106Lys)	rs141703710	0.00717
NM_058174.3(COL6A2):c.2649C>T (p.Phe883=)	rs149172490	0.00540
NM_001849.4(COL6A2):c.2980G>A (p.Ala994Thr)	rs117931394	0.00474
NM_001849.4(COL6A2):c.510C>T (p.Cys170=)	rs142328765	0.00343
NM_001849.4(COL6A2):c.2558G>A (p.Arg853Gln)	rs144830948	0.00148
NM_001849.4(COL6A2):c.1251C>T (p.Arg417=)	rs61735827

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