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

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.4855G>T (p.Glu1619Ter)	rs774067157
NM_000342.4(SLC4A1):c.1153G>C (p.Asp385His)	rs2047407019
NM_006363.6(SEC23B):c.716A>G (p.Asp239Gly)	rs761034212

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