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

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.5544+91C>T	rs72638959	0.00849
NM_006363.6(SEC23B):c.1512T>C (p.Asn504=)	rs138198461	0.00271
NM_001243177.4(ALDOA):c.1201G>A (p.Gly401Ser)	rs138824667	0.00256

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