List of variants reported as likely pathogenic for familial hemolytic anemia by Mendelics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001360016.2(G6PD):c.1366G>A (p.Asp456Asn)	rs782317415	0.00001
NM_000611.6(CD59):c.83G>A (p.Cys28Tyr)	rs1853849281
NM_001358263.1(HK1):c.1A>T (p.Met1Leu)	rs1589439508

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