Variant (rsID / SNP)
rs8065080
rs8065080 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPV1. Location: chromosome 17, position 3,480,447. The table records no clinical significance for this variant.
Reference-table entries
TRPV1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:3480447
- HGVS
- NM_018727.5,c.1753A>G,p.Ile585Val
- Allele change
- Missense_I585V
Associated conditions / phenotypes
Cough Variant Asthma|Autoimmune Disease|Migraine with or Without Aura 1|Glucose Intolerance|Osteoarthritis|Pancreatitis|T-Cell Lymphoma 1a|Chronic Pain
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.