Variant (rsID / SNP)
rs11614418
rs11614418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STAB2. Location: chromosome 12, position 104,067,812. The table records no clinical significance for this variant.
Reference-table entries
STAB2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:104067812
- HGVS
- NM_017564.10,c.2499C>T,p.Tyr833Tyr
- Allele change
- Synonymous_Y833Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.