Variant (rsID / SNP)
rs1131446
rs1131446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-B. Location: chromosome 6, position 31,323,116. The table records no clinical significance for this variant.
Reference-table entries
HLA-BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31323116
- HGVS
- NM_005514.8,c.873G>A,p.Pro291Pro
- Allele change
- Synonymous_P291P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.