List of variants reported as benign for Sengers syndrome

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Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_018238.4(AGK):c.*1175C>T	rs71545336	0.02792
NM_018238.4(AGK):c.*141C>T	rs6943245	0.01947
NM_018238.4(AGK):c.*320G>A	rs3735282	0.01469
NM_018238.4(AGK):c.*1210A>T	rs184938991	0.00966
NM_018238.4(AGK):c.*184C>T	rs116500538	0.00466
NM_018238.4(AGK):c.101+5C>T	rs150421355	0.00346
NM_018238.4(AGK):c.518+18G>A	rs192082201	0.00235
NM_018238.4(AGK):c.17A>G (p.Lys6Arg)	rs148294392	0.00226
NM_018238.4(AGK):c.297+18A>G	rs138364626	0.00225
NM_018238.4(AGK):c.424-11T>C	rs200973491	0.00044
NM_018238.4(AGK):c.1088C>T (p.Thr363Met)	rs142069429	0.00043
NM_018238.4(AGK):c.877+15G>A	rs201052151	0.00029
NM_018238.4(AGK):c.804C>T (p.Thr268=)	rs543549513	0.00006
NM_018238.4(AGK):c.619A>G (p.Thr207Ala)	rs561898521	0.00001
NM_018238.4(AGK):c.1046+13G>C
NM_018238.4(AGK):c.142-10del
NM_018238.4(AGK):c.424-3del
NM_018238.4(AGK):c.424-3dup	rs201762775
NM_018238.4(AGK):c.424-4C>A	rs113085050
NM_018238.4(AGK):c.424-4C>G	rs113085050
NM_018238.4(AGK):c.424-5C>T	rs113599212
NM_018238.4(AGK):c.669-6del
NM_018238.4(AGK):c.975+16dup

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