Variant (rsID / SNP)
rs1059510
rs1059510 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-E. Location: chromosome 6, position 30,457,732. The table records no clinical significance for this variant.
Reference-table entries
HLA-ENot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30457732
- HGVS
- NM_005516.6,c.294T>C,p.Asn98Asn
- Allele change
- Synonymous_N98N
Associated conditions / phenotypes
Rheumatoid Arthritis|Enthesopathy|Arthritis|Inflammatory Spondylopathy|Hepatitis C|Spondyloarthropathy 1|Hepatitis|Spondylitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.