Variant (rsID / SNP)
rs20575
rs20575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF10A. Location: chromosome 8, position 23,059,324. The table records no clinical significance for this variant.
Reference-table entries
TNFRSF10ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 8:23059324
- HGVS
- NM_003844.4,c.626G>C,p.Arg209Thr
- Allele change
- Missense_R209T
Associated conditions / phenotypes
Lymphoma|Follicular Lymphoma|Gallbladder Cancer|Hepatocellular Carcinoma|Liver Cirrhosis|Crohn's Disease|Alzheimer Disease|Psoriatic Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.