Variant (rsID / SNP)
rs1165196
rs1165196 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC17A1. Location: chromosome 6, position 25,813,150. The table records no clinical significance for this variant.
Reference-table entries
SLC17A1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:25813150
- HGVS
- NM_005074.5,c.806C>T,p.Thr269Ile
- Allele change
- Missense_T269I
Associated conditions / phenotypes
Gout|Atrial Fibrillation|Hyperuricemia|Hypercholesterolemia, Familial, 1|Hypertriglyceridemia 1|Polycystic Kidney Disease|Hypercholesterolemia, Familial, 3|Hypertriglyceridemia, Transient Infantile|Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease|Enthesopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.