Variant (rsID / SNP)
rs2295879
rs2295879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TACC2. Location: chromosome 10, position 123,996,976. The table records no clinical significance for this variant.
Reference-table entries
TACC2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:123996976
- HGVS
- NM_206862.4,c.8194G>A,p.Ala2732Thr
- Allele change
- Missense_A2732T
Associated conditions / phenotypes
Missense_A810T|Missense_A780T|Missense_A792T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.