ClinVar Miner

List of variants reported as uncertain significance for combined immunodeficiency due to DOCK8 deficiency by New York Genome Center

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.3023G>A (p.Arg1008Gln)	rs145844320	0.00064
NM_203447.4(DOCK8):c.494C>T (p.Ser165Leu)	rs146490788	0.00061
NM_203447.4(DOCK8):c.3312G>C (p.Glu1104Asp)	rs138810908	0.00054

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