Variant (rsID / SNP)
rs3796295
rs3796295 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNIK. Location: chromosome 3, position 171,087,469. The table records no clinical significance for this variant.
Reference-table entries
TNIKNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:171087469
- HGVS
- NM_015028.4,c.63C>T,p.Pro21Pro
- Allele change
- Synonymous_P21P
Associated conditions / phenotypes
Synonymous_P21P|Synonymous_P21P|Synonymous_P21P|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.