List of variants reported as likely pathogenic for anemia by MGZ Medical Genetics Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.1010C>T (p.Pro337Leu)	rs202153130	0.00007
NM_001374504.1(TMPRSS6):c.1297G>A (p.Gly433Arg)	rs137853119	0.00004
NM_000135.4(FANCA):c.1944del (p.Glu648fs)	rs1555549451	0.00001
NM_001355436.2(SPTB):c.5178+1G>A

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