Variant (rsID / SNP)
rs34378673
rs34378673 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPV1. Location: chromosome 17, position 3,480,910. The table records no clinical significance for this variant.
Reference-table entries
TRPV1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:3480910
- HGVS
- NM_018727.5,c.1695T>C,p.Tyr565Tyr
- Allele change
- Synonymous_Y565Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.