Variant (rsID / SNP)
rs6971
rs6971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSPO. Location: chromosome 22, position 43,558,926. The table records no clinical significance for this variant.
Reference-table entries
TSPONot classified
- Variant type
- missense_variant
- Chromosome / position
- 22:43558926
- HGVS
- NM_000714.6,c.439A>G,p.Thr147Ala
- Allele change
- Silent
Associated conditions / phenotypes
Glioblastoma|Myocardial Infarction|Anxiety|Major Affective Disorder 8|Major Affective Disorder 9|Bipolar Disorder|Alcohol Use Disorder|Glioma|Glial Tumor|Alzheimer Disease|Multiple Sclerosis|Schizophrenia|Alcohol Dependence|Mild Cognitive Impairment|Rheumatoid Arthritis|Toxic Encephalopathy|Fibromyalgia|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.