List of variants reported as risk factor for anemia

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000969.5(RPL5):c.189+267G>C	rs138979590	0.00053
NM_000186.4(CFH):c.3628C>T (p.Arg1210Cys)	rs121913059	0.00019
NM_000186.4(CFH):c.3514G>T (p.Glu1172Ter)	rs121913060	0.00001
NM_000186.4(CFH):c.2697T>A (p.Tyr899Ter)	rs121913057
NM_000186.4(CFH):c.3566T>G (p.Leu1189Arg)	rs121913055
NM_000186.4(CFH):c.3572C>T (p.Ser1191Leu)	rs460897
NM_000186.4(CFH):c.3592G>T (p.Glu1198Ter)	rs121913063
NM_000186.4(CFH):c.3643C>G (p.Arg1215Gly)	rs121913051
NM_000186.4(CFH):c.3677_*4del (p.Pro1226_Ter1232delinsXaa)	rs796052136
NM_000186.4(CFH):c.83_86del (p.Arg28fs)	rs796052137
NM_015937.6(PIGT):c.1401-2A>G	rs587777028
NM_015937.6(PIGT):c.197del (p.Tyr66fs)	rs1555876283
NM_015937.6(PIGT):c.767_770del (p.Lys256fs)	rs776974834

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