ClinVar Miner

List of variants reported as uncertain significance for anemia (disease) by Mayo Clinic Genetic Testing Laboratories,Mayo Clinic

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000135.4(FANCA):c.577C>G (p.Leu193Val) rs141861208
NM_000291.4(PGK1):c.248T>C (p.Val83Ala) rs138851144
NM_003126.4(SPTA1):c.373G>A (p.Ala125Thr) rs201771255
NM_005334.3(HCFC1):c.4315A>C (p.Asn1439His) rs782138046
NM_015937.6(PIGT):c.949A>G (p.Ile317Val) rs773624614
NM_198253.2(TERT):c.142C>G (p.Arg48Gly) rs1554043151

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