List of variants reported as uncertain significance for Familial hemolytic anemia by Department of Genetic, Henri Mondor Hospital, Assistance Publique des Hôpitaux de Paris

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_003126.4(SPTA1):c.1688G>A (p.Arg563Gln)	rs202243588	0.00032
NM_000064.4(C3):c.1921G>A (p.Asp641Asn)	rs1348311492
NM_001142864.4(PIEZO1):c.1126C>G (p.Pro376Ala)	rs1474972037
NM_001355436.2(SPTB):c.6706C>A (p.Leu2236Met)	rs1555364746
NM_001355436.2(SPTB):c.6737C>T (p.Ala2246Val)	rs1555364743
NM_022437.3(ABCG8):c.-27G>A	rs779984848
NM_172351.3(CD46):c.402T>G (p.Ile134Met)	rs1553250568

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