Variant (rsID / SNP)
rs7488309
rs7488309 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VSIG10. Location: chromosome 12, position 118,520,170. The table records no clinical significance for this variant.
Reference-table entries
VSIG10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:118520170
- HGVS
- NM_019086.6,c.426C>T,p.Tyr142Tyr
- Allele change
- Synonymous_Y142Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.