List of variants studied for congenital nonspherocytic hemolytic anemia by 3billion

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000298.6(PKLR):c.1456C>T (p.Arg486Trp)	rs116100695	0.00270
NM_000402.4(G6PD):c.653C>T (p.Ser218Phe)	rs5030868	0.00028
NM_000175.5(GPI):c.671C>T (p.Thr224Met)	rs61754634	0.00005
NM_000298.6(PKLR):c.1178A>G (p.Asn393Ser)	rs776594413	0.00001
NM_000298.6(PKLR):c.1217G>A (p.Gly406Glu)	rs779817999	0.00001
NM_000175.5(GPI):c.1238A>G (p.Gln413Arg)
NM_000298.6(PKLR):c.1015G>A (p.Asp339Asn)	rs747097960
NM_000298.6(PKLR):c.1015del (p.Asp339fs)	rs1193689718
NM_000298.6(PKLR):c.1061A>G (p.Lys354Arg)	rs2148204121
NM_000298.6(PKLR):c.1575G>A (p.Trp525Ter)	rs2148198897
NM_000298.6(PKLR):c.227T>C (p.Leu76Pro)
NM_000298.6(PKLR):c.451G>A (p.Val151Met)
NM_000298.6(PKLR):c.694+43C>T
NM_000298.6(PKLR):c.808C>T (p.Arg270Ter)
NM_000298.6(PKLR):c.945G>C (p.Glu315Asp)	rs2148204818
NM_000402.4(G6PD):c.1268G>A (p.Arg423His)	rs137852316

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