Variant (rsID / SNP)
rs1131532
rs1131532 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF10. Location: chromosome 3, position 172,224,303. The table records no clinical significance for this variant.
Reference-table entries
TNFSF10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:172224303
- HGVS
- NM_003810.4,c.825T>C,p.Phe275Phe
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.