List of variants reported as likely pathogenic for familial hemolytic anemia by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.2632G>T (p.Glu878Ter)
NM_000298.6(PKLR):c.829G>T (p.Glu277Ter)
NM_001355436.2(SPTB):c.3784_3787del (p.Lys1262fs)	rs1594773586

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