Variant (rsID / SNP)
rs2734849
rs2734849 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKK1. Location: chromosome 11, position 113,270,160. The table records no clinical significance for this variant.
Reference-table entries
ANKK1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:113270160
- HGVS
- NM_178510.2,c.1469A>G,p.His490Arg
- Allele change
- Missense_H490R
Associated conditions / phenotypes
Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Hyperprolactinemia|Brain Injury|Traumatic Brain Injury
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.