List of variants reported as pathogenic for familial hemolytic anemia by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000365.6(TPI1):c.315G>C (p.Glu105Asp)	rs121964845	0.00012
NM_003126.4(SPTA1):c.779T>C (p.Leu260Pro)	rs121918634	0.00006

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