List of variants studied for anemia by Institute of Human Genetics, Cologne University

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.2658G>C (p.Glu886Asp)	rs139002130	0.00055
NM_000135.4(FANCA):c.1367T>C (p.Phe456Ser)
NM_000135.4(FANCA):c.2749C>T (p.Arg917Ter)	rs1060501880
NM_000186.4(CFH):c.1616G>T (p.Gly539Val)	rs1027258331
NM_000186.4(CFH):c.2397del (p.Glu800fs)	rs1131690796
NM_000186.4(CFH):c.2950T>C (p.Cys984Arg)	rs886039869
NM_000186.4(CFH):c.2975T>G (p.Leu992Ter)

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