Variant (rsID / SNP)
rs3810936
rs3810936 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF15. Location: chromosome 9, position 117,552,885. The table records no clinical significance for this variant.
Reference-table entries
TNFSF15Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:117552885
- HGVS
- NM_005118.4,c.603A>G,p.Val201Val
- Allele change
- Synonymous_V201V
Associated conditions / phenotypes
Crohn's Disease|Colitis|Ulcerative Colitis|Autoimmune Disease|Systemic Lupus Erythematosus|Lupus Erythematosus|Exanthem|Inflammatory Spondylopathy|Graves' Disease|Spondyloarthropathy 1|Spondylitis|Inflammatory Bowel Disease|Uveitis|Rheumatoid Arthritis|Sjogren Syndrome|Diverticulitis|Iridocyclitis|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.