Variant (rsID / SNP)
rs282129
rs282129 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GABRR2. Location: chromosome 6, position 89,967,498. The table records no clinical significance for this variant.
Reference-table entries
GABRR2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:89967498
- HGVS
- NM_002043.5,c.1289C>T,p.Thr430Met
- Allele change
- Missense_T430M
Associated conditions / phenotypes
Restless Legs Syndrome|Alcohol Dependence|Migraine with or Without Aura 1|Essential Tremor|Tremor
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.