Variant (rsID / SNP)
rs2536512
rs2536512 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOD3. Location: chromosome 4, position 24,801,315. The table records no clinical significance for this variant.
Reference-table entries
SOD3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:24801315
- HGVS
- NM_003102.4,c.172G>A,p.Ala58Thr
- Allele change
- Missense_A58T
Associated conditions / phenotypes
Hypertension, Essential|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Hypertriglyceridemia 1|Gastric Cancer|Hypertriglyceridemia, Transient Infantile|Type 2 Diabetes Mellitus|Rheumatoid Arthritis|Melanoma|Diabetes Mellitus|Lipid Metabolism Disorder|Malaria|Drug-Induced Hepatitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.