ClinVar Miner

List of variants reported as likely benign for anemia (disease) by Johns Hopkins Genomics,Johns Hopkins University

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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NM_001143992.1(WRAP53):c.807C>T (p.Arg269=) rs35307405
NM_001363.5(DKC1):c.1512_1514delGAA (p.Lys505del) rs782576893
NM_001363.5(DKC1):c.369G>T (p.Thr123=) rs2728532
NM_018081.2(WRAP53):c.1359C>T (p.Pro453=) rs35082161
NM_198253.2(TERT):c.2517G>A (p.Thr839=) rs140124989
NM_198253.2(TERT):c.604G>A (p.Ala202Thr) rs121918661

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