Variant (rsID / SNP)
rs2292334
rs2292334 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A3. Location: chromosome 6, position 160,858,188. The table records no clinical significance for this variant.
Reference-table entries
SLC22A3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:160858188
- HGVS
- NM_021977.4,c.1233G>A,p.Ala411Ala
- Allele change
- Synonymous_A411A
Associated conditions / phenotypes
Type 2 Diabetes Mellitus|Diabetes Mellitus|Cholestasis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.