Variant (rsID / SNP)
rs860170
rs860170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R16. Location: chromosome 7, position 122,635,024. The table records no clinical significance for this variant.
Reference-table entries
TAS2R16Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:122635024
- HGVS
- NM_016945.3,c.665G>A,p.Arg222His
- Allele change
- Missense_R222H
Associated conditions / phenotypes
Colorectal Cancer|Rectum Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.