Variant (rsID / SNP)
rs2305089
rs2305089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBXT. Location: chromosome 6, position 166,579,270. The table records no clinical significance for this variant.
Reference-table entries
TBXTNot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:166579270
- HGVS
- NM_001366285.2,c.530G>A,p.Gly177Asp
- Allele change
- Missense_G177D
Associated conditions / phenotypes
Chordoma|Bone Cancer|Chronic Asthma|Asthma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.