List of variants reported as benign for Autosomal recessive limb-girdle muscular dystrophy type 2K

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001077365.2(POMT1):c.856-49T>G	rs4740163	0.97653
NM_001077365.2(POMT1):c.986+49G>A	rs10901066	0.88278
NM_001077365.2(POMT1):c.876T>C (p.Thr292=)	rs10901065	0.88277
NM_001077365.2(POMT1):c.1047T>C (p.Asp349=)	rs3739494	0.88273
NM_001077365.2(POMT1):c.428-21T>C	rs11243404	0.88267
NM_001077365.2(POMT1):c.700-48A>G	rs2018621	0.88264
NM_001077365.2(POMT1):c.*226T>C	rs3824395	0.88255
NM_001077365.2(POMT1):c.699+53A>G	rs2296949	0.88248
NM_001077365.2(POMT1):c.*41T>C	rs3739495	0.88174
NM_001077365.2(POMT1):c.*278T>C	rs10793885	0.88104
NM_001077365.2(POMT1):c.*348C>T	rs7857419	0.87122
NM_001077365.2(POMT1):c.1698+48C>G	rs2277152	0.84050
NM_001077365.2(POMT1):c.2003+13C>T	rs4740165	0.84044
NM_001077365.2(POMT1):c.*453T>C	rs11005	0.70594
NM_001077365.2(POMT1):c.1082+16G>A	rs59515295	0.14451
NM_001077365.2(POMT1):c.699+52C>T	rs3887873	0.12205
NM_001077365.2(POMT1):c.*421G>A	rs10257	0.11588
NM_001077365.2(POMT1):c.913G>A (p.Val305Ile)	rs4740164	0.04243
NM_001077365.2(POMT1):c.1233C>A (p.Asp411Glu)	rs11243406	0.04069
NM_001077365.2(POMT1):c.1692G>A (p.Arg564=)	rs34954751	0.02208
NM_001077365.2(POMT1):c.1275A>G (p.Glu425=)	rs62620174	0.02004
NM_001077365.2(POMT1):c.*529G>A	rs116005066	0.01991
NM_001077365.2(POMT1):c.891G>A (p.Leu297=)	rs76109289	0.00616
NM_001077365.2(POMT1):c.1545C>G (p.Ser515Arg)	rs150367385	0.00114
NM_001077365.2(POMT1):c.*285A>G	rs4740259
NM_001077365.2(POMT1):c.123-5dup	rs148086540

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