List of variants reported as likely benign for blood coagulation disease by Genome-Nilou Lab

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.1717-48A>G	rs5966	0.06916
NM_000186.4(CFH):c.3148A>T (p.Asn1050Tyr)	rs35274867	0.01982
NM_000186.4(CFH):c.2634C>T (p.His878=)	rs35292876	0.00829
NM_000186.4(CFH):c.3050C>T (p.Thr1017Ile)	rs34362004	0.00426
NM_032383.5(HPS3):c.2055G>A (p.Leu685=)	rs140443498	0.00300
NM_000186.4(CFH):c.1707C>T (p.Cys569=)	rs144976181	0.00129
NM_000133.4(F9):c.19A>T (p.Ile7Phe)	rs150190385	0.00086
NM_000186.4(CFH):c.2509G>A (p.Val837Ile)	rs55807605	0.00050
NM_000186.4(CFH):c.2637A>G (p.Gly879=)	rs55752475	0.00050
NM_000186.4(CFH):c.2821G>T (p.Val941Phe)	rs529491401	0.00039
NM_000186.4(CFH):c.245-8C>T	rs537160602	0.00038
NM_000186.4(CFH):c.3172T>C (p.Tyr1058His)	rs55679475	0.00029
NM_000186.4(CFH):c.3178G>C (p.Val1060Leu)	rs55771831	0.00029
NM_000186.4(CFH):c.3318A>G (p.Thr1106=)	rs1137971	0.00009
NM_000186.4(CFH):c.2056+16T>C	rs777352172	0.00006
NM_000186.4(CFH):c.245-17T>A	rs775088366	0.00006
NM_000186.4(CFH):c.2085T>A (p.Pro695=)	rs777482186	0.00005
NM_000186.4(CFH):c.59-16T>C	rs201067374	0.00005
NM_000186.4(CFH):c.2236+18A>G	rs749643506	0.00004
NM_000186.4(CFH):c.2957-15T>C	rs756514818	0.00004
NM_000186.4(CFH):c.964+18C>A	rs1258420173	0.00004
NM_000186.4(CFH):c.2868G>A (p.Thr956=)	rs533238588	0.00003
NM_000186.4(CFH):c.2427A>G (p.Gln809=)	rs758809077	0.00002
NM_000186.4(CFH):c.906C>G (p.Thr302=)	rs148552495	0.00002
NM_000186.4(CFH):c.2236+10C>G	rs755790229	0.00001
NM_000186.4(CFH):c.2946A>G (p.Pro982=)	rs553471643	0.00001
NM_000186.4(CFH):c.849A>G (p.Lys283=)	rs771886590	0.00001
NM_000128.4(F11):c.1481-34G>T	rs2289253
NM_000128.4(F11):c.1576+51C>A	rs2289254
NM_000186.4(CFH):c.1617T>C (p.Gly539=)
NM_000186.4(CFH):c.1935G>A (p.Thr645=)	rs56035657
NM_000186.4(CFH):c.2783-3dup	rs748791414
NM_000186.4(CFH):c.318T>C (p.Tyr106=)	rs1448752091

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