ClinVar Miner

List of variants in gene PIGT reported as uncertain significance for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_015937.6(PIGT):c.602T>C (p.Leu201Pro) rs1555876854
NM_015937.6(PIGT):c.634C>T (p.His212Tyr) rs574183358
NM_015937.6(PIGT):c.949A>G (p.Ile317Val) rs773624614

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