ClinVar Miner

List of variants in gene combination RTEL1, RTEL1-TNFRSF6B reported as uncertain significance for acquired aplastic anemia

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_032957.4(RTEL1):c.2702_2704delAGA (p.Lys901del) rs1555812473

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