Variant (rsID / SNP)
rs4246905
rs4246905 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF15. Location: chromosome 9, position 117,553,249. The table records no clinical significance for this variant.
Reference-table entries
TNFSF15Not classified
- Variant type
- intron_variant
- Chromosome / position
- 9:117553249
- HGVS
- NM_005118.4,c.302-63A>G
- Allele change
- Silent
Associated conditions / phenotypes
Graves' Disease|Autoimmune Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.