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

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001360016.2(G6PD):c.968T>C (p.Leu323Pro)	rs76723693	0.00154
NM_000298.6(PKLR):c.1082A>C (p.Asn361Thr)	rs1358047518	0.00001
G6PD NARA	rs587776730

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