List of variants reported as uncertain significance for familial hemolytic anemia by Mendelics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000298.6(PKLR):c.1269+43T>C	rs8177982	0.00718
NM_001355436.2(SPTB):c.3679C>T (p.Pro1227Ser)	rs149186357	0.00141
NM_006363.6(SEC23B):c.74C>A (p.Pro25His)	rs6045440	0.00050
NM_000402.4(G6PD):c.556G>A (p.Glu186Lys)	rs137852313	0.00016
NM_000402.4(G6PD):c.1114C>T (p.Leu372Phe)	rs137852342	0.00003
NM_003126.4(SPTA1):c.6421C>T (p.Arg2141Trp)	rs41273519

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