Variant (rsID / SNP)
rs762178
rs762178 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OLIG2. Location: chromosome 21, position 34,399,401. The table records no clinical significance for this variant.
Reference-table entries
OLIG2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:34399401
- HGVS
- NM_005806.4,c.231A>G,p.Ser77Ser
- Allele change
- Synonymous_S77S
Associated conditions / phenotypes
Obsessive-Compulsive Disorder|Mood Disorder|Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.