Variant (rsID / SNP)
rs7589474
rs7589474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK10. Location: chromosome 2, position 225,727,431. The table records no clinical significance for this variant.
Reference-table entries
DOCK10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:225727431
- HGVS
- NM_001363762.1,c.1674A>G,p.Gln558Gln
- Allele change
- Synonymous_Q545Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
