ClinVar Miner

List of variants studied for B cell deficiency by Service de Génétique Moléculaire, Hôpital Robert Debré

Included ClinVar conditions (64):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.2400C>A (p.Phe800Leu)

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