Variant (rsID / SNP)
rs12356193
rs12356193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A9. Location: chromosome 10, position 61,413,353. The table records no clinical significance for this variant.
Reference-table entries
SLC16A9Not classified
- Variant type
- intron_variant
- Chromosome / position
- 10:61413353
- HGVS
- NM_001323981.2,c.1351+80T>C
- Allele change
- Silent
Associated conditions / phenotypes
Hepatitis a|Hepatitis B|Hepatitis|Gout|Lipoprotein Quantitative Trait Locus|Dementia|Arteries, Anomalies of|Hyperuricemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.