Variant (rsID / SNP)
rs6275
rs6275 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRD2. Location: chromosome 11, position 113,283,477. Clinical significance in the table: Benign.
Reference-table entries
DRD2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:113283477
- Cytoband
- 11q23.2
- HGVS
- NM_000795.4(DRD2):c.939T>C (p.His313=)
- Allele change
- Synonymous_H313H
Associated conditions / phenotypes
Dystonic disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.