Variant (rsID / SNP)
rs1061235
rs1061235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-A. Location: chromosome 6, position 29,913,298. Clinical significance in the table: risk factor.
Reference-table entries
HLA-ARisk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:29913298
- Cytoband
- 6p22.1
- HGVS
- NM_001242758.1(HLA-A):c.*66A>T
- Allele change
- Silent
Associated conditions / phenotypes
Carbamazepine hypersensitivity
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.