List of variants in gene DOCK8 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.53+52T>G	rs192260189	0.01354
NM_203447.4(DOCK8):c.3840+3A>G	rs16938572	0.00865
NM_203447.4(DOCK8):c.5962-38_5962-17del	rs771454295

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