List of variants reported as benign for Autosomal recessive limb-girdle muscular dystrophy type 2N by Illumina Laboratory Services, Illumina

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_013382.7(POMT2):c.*1742G>A	rs12894594	0.83615
NM_013382.7(POMT2):c.*1501G>A	rs4141640	0.83310
NM_013382.7(POMT2):c.*1137G>A	rs7158951	0.56341
NM_013382.7(POMT2):c.*790G>A	rs7159558	0.56247
NM_013382.7(POMT2):c.*1058G>A	rs11624564	0.41162
NM_013382.7(POMT2):c.*1967C>T	rs11547794	0.41103
NM_013382.7(POMT2):c.*1974G>A	rs11159254	0.41096
NM_013382.7(POMT2):c.-64G>A	rs2270421	0.24706
NM_013382.7(POMT2):c.*2325A>G	rs11547793	0.22179
NM_013382.7(POMT2):c.*75C>T	rs1055592	0.20469
NM_013382.7(POMT2):c.*1516A>G	rs45518539	0.14946
NM_013382.7(POMT2):c.*587G>A	rs10141995	0.14409
NM_013382.7(POMT2):c.*1748C>A	rs45458096	0.11420
NM_013382.7(POMT2):c.-124G>A	rs147337187	0.06001
NM_013382.7(POMT2):c.162G>T (p.Ala54=)	rs2270420	0.05519
NM_013382.7(POMT2):c.-128C>T	rs116224770	0.03577
NM_013382.7(POMT2):c.161C>A (p.Ala54Glu)	rs8177536	0.03119
NM_013382.7(POMT2):c.*1087C>T	rs59725094	0.01993
NM_013382.7(POMT2):c.2175C>T (p.Tyr725=)	rs116434191	0.00658

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