List of variants reported as benign for Myosclerosis

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_001849.4(COL6A2):c.1671+10A>G	rs915786	0.86241
NM_001849.4(COL6A2):c.1332+26A>G	rs3737362	0.82158
NM_001849.4(COL6A2):c.1771-25A>G	rs2839113	0.81072
NM_001849.4(COL6A2):c.1196G>A (p.Ser399Asn)	rs2839110	0.74122
NM_001849.4(COL6A2):c.2462-35C>T	rs7279622	0.54180
NM_001849.4(COL6A2):c.1116+32G>A	rs7279347	0.49217
NM_001849.4(COL6A2):c.2039G>A (p.Arg680His)	rs1042917	0.45419
NM_001849.4(COL6A2):c.928-19C>T	rs762438	0.45414
NM_001849.4(COL6A2):c.2097C>T (p.Gly699=)	rs13046639	0.44460
NM_001849.4(COL6A2):c.2094G>A (p.Ala698=)	rs13052956	0.44458
NM_001849.4(COL6A2):c.2184G>A (p.Val728=)	rs2839114	0.32526
NM_001849.4(COL6A2):c.1333-8T>C	rs73159701	0.17496
NM_001849.4(COL6A2):c.2979C>T (p.Arg993=)	rs6652	0.14487
NM_001849.4(COL6A2):c.2724A>G (p.Thr908=)	rs9977394	0.13855
NM_001849.4(COL6A2):c.1609-10C>T	rs17357592	0.11879
NM_001849.4(COL6A2):c.663C>T (p.Pro221=)	rs59531343	0.09859
NM_206965.2(FTCD):c.1470C>T (p.Gly490=)	rs10432965	0.09606
NM_001849.4(COL6A2):c.*116T>C	rs3087667	0.08255
NM_001849.4(COL6A2):c.2803G>A (p.Gly935Arg)	rs35548026	0.08193
NM_001849.4(COL6A2):c.*158C>T	rs11554666	0.06989
NM_001849.4(COL6A2):c.1770+4G>A	rs9981981	0.06098
NM_001849.4(COL6A2):c.2163G>A (p.Gln721=)	rs16978875	0.03433
NM_001849.4(COL6A2):c.3043A>C (p.Ile1015Leu)	rs11910483	0.02152
NM_001849.4(COL6A2):c.2980G>A (p.Ala994Thr)	rs117931394	0.00474
NM_001849.4(COL6A2):c.*119A>G	rs1043962
NM_001849.4(COL6A2):c.1672-24C>G	rs3746995
NM_001849.4(COL6A2):c.1817-3dup	rs149954350

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