rs1427676
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1427676(C;C) |
Make rs1427676(C;T) |
Make rs1427676(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 203876443 |
is a | snp |
is | mentioned by |
dbSNP | rs1427676 |
dbSNP (classic) | rs1427676 |
ClinGen | rs1427676 |
ebi | rs1427676 |
HLI | rs1427676 |
Exac | rs1427676 |
Gnomad | rs1427676 |
Varsome | rs1427676 |
LitVar | rs1427676 |
Map | rs1427676 |
PheGenI | rs1427676 |
Biobank | rs1427676 |
1000 genomes | rs1427676 |
hgdp | rs1427676 |
ensembl | rs1427676 |
geneview | rs1427676 |
scholar | rs1427676 |
rs1427676 | |
pharmgkb | rs1427676 |
gwascentral | rs1427676 |
openSNP | rs1427676 |
23andMe | rs1427676 |
SNPshot | rs1427676 |
SNPdbe | rs1427676 |
MSV3d | rs1427676 |
GWAS Ctlg | rs1427676 |
GMAF | 0.4582 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19956106] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families
[PMID 19956097] Remapping the type I diabetes association of the CTLA4 locus.
[PMID 19956101] Overview of the Rapid Response data.
[PMID 20537165] The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease.