ClinVar Miner

List of variants reported as uncertain significance for Common variable immunodeficiency by NIHR Bioresource Rare Diseases, University of Cambridge

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000074.3(CD40LG):c.98T>A (p.Ile33Asn) rs1283517835

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