Variant (rsID / SNP)
rs1129055
rs1129055 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD86. Location: chromosome 3, position 121,838,319. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 3:121838319
- HGVS
- NM_175862.5,c.928G>A,p.Ala310Thr
- Allele change
- Missense_A198T
Associated conditions / phenotypes
Pemphigus Vulgaris, Familial|Pemphigus|Pemphigus Foliaceus|Lipoprotein Quantitative Trait Locus|Autoimmune Disease|Pancreatic Cancer|Arteries, Anomalies of|Sarcoma|Brucellosis|Rheumatoid Arthritis|Osteogenic Sarcoma|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Pulmonary Disease, Chronic Obstructive|Spindle Cell Sarcoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.