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

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Total variants: 5

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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_001032.5(RPS29):c.149T>C (p.Ile50Thr)	rs587777569
NM_006363.6(SEC23B):c.716A>G (p.Asp239Gly)	rs761034212
NM_182916.3(TRNT1):c.608G>A (p.Arg203Lys)	rs750995691

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