List of variants reported as pathogenic for familial hemolytic anemia by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006363.6(SEC23B):c.325G>A (p.Glu109Lys)	rs121918221	0.00024
NM_006363.6(SEC23B):c.689+1G>A	rs398124226	0.00003
NM_003126.4(SPTA1):c.2320C>T (p.Arg774Ter)	rs751026146	0.00001
NM_000402.4(G6PD):c.1466G>C (p.Arg489Pro)	rs72554665

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