Variant (rsID / SNP)
rs3135391
rs3135391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-DRA. Location: chromosome 6, position 32,410,987. The table records no clinical significance for this variant.
Reference-table entries
HLA-DRANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:32410987
- HGVS
- NM_019111.5,c.354A>G,p.Thr118Thr
- Allele change
- Synonymous_T118T
Associated conditions / phenotypes
Multiple Sclerosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.