Variant (rsID / SNP)

rs2271111

rs2271111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK5. Location: chromosome 8, position 25,222,165. The table records no clinical significance for this variant.

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Reference-table entries

DOCK5Not classified

Variant type: missense_variant
Chromosome / position: 8:25222165
HGVS: NM_024940.8,c.3068A>G,p.Gln1023Arg
Allele change: Missense_Q1023R

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.