List of variants reported as likely pathogenic for familial hemolytic anemia by Illumina Laboratory Services, Illumina

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.2140C>T (p.Arg714Trp)	rs80338696	0.00008
NM_000298.6(PKLR):c.391_393del (p.Ile131del)	rs886045351
NM_138477.4(CDAN1):c.2173C>T (p.Arg725Trp)	rs138334226

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