Variant (rsID / SNP)

rs184867151

rs184867151 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK8. Location: chromosome 9, position 443,420. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DOCK8Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:443420
Cytoband: 9p24.3
HGVS: NM_203447.4(DOCK8):c.5491-7T>A
Allele change: Silent

Associated conditions / phenotypes

Combined immunodeficiency due to DOCK8 deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.