List of variants reported as pathogenic for anemia by Johns Hopkins Genomics, Johns Hopkins University

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000402.4(G6PD):c.292G>A (p.Val98Met)	rs1050828	0.03616
NM_000135.4(FANCA):c.3349A>G (p.Arg1117Gly)	rs149277003	0.00006
NM_017875.4(SLC25A38):c.832C>T (p.Arg278Ter)	rs147431446	0.00004
NM_000135.4(FANCA):c.1734_1739del (p.Tyr578_Val580delinsTer)	rs757504102	0.00001
NM_001022.4(RPS19):c.295_296delinsCAGCCGA (p.Val99fs)	rs2074119405

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