List of variants reported as likely benign for familial hemolytic anemia by Revvity Omics, Revvity

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.1483A>C (p.Asn495His)	rs143839208	0.00057
NM_000037.4(ANK1):c.4105-5T>G	rs768183148	0.00006
NM_000637.5(GSR):c.13C>T (p.Pro5Ser)
NM_001114134.2(EPB42):c.1280G>A (p.Arg427His)
NM_001114134.2(EPB42):c.2044G>A (p.Val682Ile)
NM_001367805.3(KIF23):c.497A>C (p.Glu166Ala)
NM_001376013.1(EPB41):c.832G>A (p.Val278Ile)

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