ClinVar Miner

List of variants reported as uncertain significance for combined immunodeficiency due to DOCK8 deficiency by Service de Génétique Moléculaire, Hôpital Robert Debré

Included ClinVar conditions (1):

Combined immunodeficiency due to DOCK8 deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		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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