List of variants reported as likely pathogenic for anemia by Centogene AG - the Rare Disease Company

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.156C>G (p.Phe52Leu)	rs80338694	0.00009
NM_000402.4(G6PD):c.577G>A (p.Gly193Ser)	rs137852314
NM_005431.2(XRCC2):c.350dup (p.Leu117fs)	rs764640893
NM_022725.4(FANCF):c.817_820del (p.Val273fs)	rs1858619779

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