rs1129055
Orientation | plus |
Stabilized | plus |
Make rs1129055(A;A) |
Make rs1129055(A;G) |
Make rs1129055(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 122119472 |
Gene | CD86 |
is a | snp |
is | mentioned by |
dbSNP | rs1129055 |
dbSNP (classic) | rs1129055 |
ClinGen | rs1129055 |
ebi | rs1129055 |
HLI | rs1129055 |
Exac | rs1129055 |
Gnomad | rs1129055 |
Varsome | rs1129055 |
LitVar | rs1129055 |
Map | rs1129055 |
PheGenI | rs1129055 |
Biobank | rs1129055 |
1000 genomes | rs1129055 |
hgdp | rs1129055 |
ensembl | rs1129055 |
geneview | rs1129055 |
scholar | rs1129055 |
rs1129055 | |
pharmgkb | rs1129055 |
gwascentral | rs1129055 |
openSNP | rs1129055 |
23andMe | rs1129055 |
SNPshot | rs1129055 |
SNPdbe | rs1129055 |
MSV3d | rs1129055 |
GWAS Ctlg | rs1129055 |
GMAF | 0.3324 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21563968] CD86?+?1057G/A Polymorphism and Susceptibility to Osteosarcoma
[PMID 20230296] Absence of association between CD86 +1057G/A polymorphism and coronary artery disease.
[PMID 20732370] CTLA4 and CD86 gene polymorphisms and susceptibility to chronic obstructive pulmonary disease.
[PMID 21870962] CD86 +1057G/A polymorphism and susceptibility to Ewing's sarcoma: a case-control study.
[PMID 23661460] CTLA-4 and CD86 genetic variants and haplotypes in patients with rheumatoid arthritis in southeastern China
[PMID 24298899] Investigation of CTLA-4 and CD86 gene polymorphisms in a group of Iranian patients with brucellosis infection
[PMID 22821131] CD86 gene variants and susceptibility to pancreatic cancer.
[PMID 29577049] The Influence of Genetic Variations in the CD86 Gene on the Outcome after Allogeneic Hematopoietic Stem Cell Transplantation.
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d