List of variants reported as uncertain significance for familial hemolytic anemia by Centogene AG - the Rare Disease Company

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003126.4(SPTA1):c.1982G>A (p.Arg661His)	rs201845149	0.00134
NM_003126.4(SPTA1):c.3357G>C (p.Lys1119Asn)	rs200230894	0.00098
NM_002250.3(KCNN4):c.1007C>T (p.Ala336Val)	rs141341073	0.00001
NM_138477.4(CDAN1):c.2174G>A (p.Arg725Gln)	rs962870388	0.00001
NM_003126.4(SPTA1):c.6421C>T (p.Arg2141Trp)	rs41273519

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