Variant (rsID / SNP)
rs1048101
rs1048101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADRA1A. Location: chromosome 8, position 26,628,028. The table records no clinical significance for this variant.
Reference-table entries
ADRA1ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 8:26628028
- HGVS
- NM_033303.4,c.1039T>C,p.Cys347Arg
- Allele change
- Silent
Associated conditions / phenotypes
Hypertension, Essential|Fibromyalgia|Complex Regional Pain Syndrome|Cocaine Abuse|Cocaine Dependence|Heart Disease|Syncope
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.