List of variants reported as uncertain significance for anemia by MGZ Medical Genetics Center

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001374504.1(TMPRSS6):c.844G>A (p.Gly282Ser)	rs145053404	0.00081
NM_015506.3(MMACHC):c.181C>T (p.Arg61Trp)	rs200483477	0.00072
NM_000518.5(HBB):c.93G>T (p.Arg31Ser)	rs1135071	0.00035
NM_000096.4(CP):c.1039G>A (p.Gly347Ser)	rs761317252	0.00001
NM_000791.4(DHFR):c.335T>G (p.Met112Arg)
NM_001081.4(CUBN):c.2446G>A (p.Ala816Thr)
NM_003126.4(SPTA1):c.6592G>A (p.Ala2198Thr)
NM_015506.3(MMACHC):c.792_818del (p.Ser264_Pro272del)	rs753855245

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