Variant (rsID / SNP)
rs12328236
rs12328236 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK10. Location: chromosome 2, position 225,672,460. The table records no clinical significance for this variant.
Reference-table entries
DOCK10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:225672460
- HGVS
- NM_001363762.1,c.3666C>T,p.Tyr1222Tyr
- Allele change
- Synonymous_Y1209Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
