Variant (rsID / SNP)
rs240226
rs240226 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTK. Location: chromosome 6, position 80,715,838. The table records no clinical significance for this variant.
Reference-table entries
TTKNot classified
- Variant type
- intron_variant
- Chromosome / position
- 6:80715838
- HGVS
- NM_003318.5,c.139+139T>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.