List of variants reported as uncertain significance for familial hemolytic anemia by 3billion, Medical Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000342.4(SLC4A1):c.2002G>A (p.Ala668Thr)	rs368353943	0.00002
NM_000298.6(PKLR):c.1217G>A (p.Gly406Glu)	rs779817999	0.00001
NM_006363.6(SEC23B):c.1385A>G (p.Tyr462Cys)	rs780978419	0.00001
NM_000037.4(ANK1):c.2389-8C>A
NM_000175.5(GPI):c.1238A>G (p.Gln413Arg)
NM_000298.6(PKLR):c.1061A>G (p.Lys354Arg)	rs2148204121
NM_000298.6(PKLR):c.1575G>A (p.Trp525Ter)	rs2148198897
NM_000298.6(PKLR):c.227T>C (p.Leu76Pro)
NM_000298.6(PKLR):c.451G>A (p.Val151Met)
NM_000298.6(PKLR):c.694+43C>T
NM_000298.6(PKLR):c.945G>C (p.Glu315Asp)	rs2148204818
NM_000342.4(SLC4A1):c.1319T>A (p.Leu440Gln)	rs2144613306
NM_000365.6(TPI1):c.694G>A (p.Val232Met)	rs1555132614
NM_001376013.1(EPB41):c.1604C>T (p.Ala535Val)
NM_003126.4(SPTA1):c.1007C>T (p.Ser336Leu)	rs2101929378

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