ClinVar Miner

List of variants in gene combination DOCK8, LOC126860552 reported as benign for combined immunodeficiency due to DOCK8 deficiency

Included ClinVar conditions (1):

Combined immunodeficiency due to DOCK8 deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.289C>A (p.Pro97Thr)	rs529208	0.47790
NM_203447.4(DOCK8):c.187G>A (p.Asp63Asn)	rs3209441	0.11431

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