List of variants reported as pathogenic for anemia by Intergen, Intergen Genetics and Rare Diseases Diagnosis Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.653C>T (p.Ser218Phe)	rs5030868	0.00028
NM_000518.5(HBB):c.93-21G>A	rs35004220	0.00009
NM_000402.4(G6PD):c.1039G>A (p.Glu347Lys)	rs137852339	0.00004
NM_000402.4(G6PD):c.1093G>A (p.Ala365Thr)	rs5030869	0.00003
NM_000402.4(G6PD):c.1466G>C (p.Arg489Pro)	rs72554665

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