Variant (rsID / SNP)
rs316019
rs316019 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A2. Location: chromosome 6, position 160,670,282. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 6:160670282
- HGVS
- NM_003058.4,c.808T>G,p.Ser270Ala
- Allele change
- Missense_S270A
Associated conditions / phenotypes
Lactic Acidosis|Anoxia|Sensorineural Hearing Loss|Wolfram Syndrome 1|Lung Cancer|Type 2 Diabetes Mellitus|Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus|Diabetes Mellitus|Testicular Cancer|Branchiootic Syndrome 1|Polycystic Ovary Syndrome|Body Mass Index Quantitative Trait Locus 1|Type 1 Diabetes Mellitus|Colorectal Cancer|Rheumatoid Arthritis|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.