rs17166496
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 1.1x risk for type-1 diabetes | |
(C;G) | 0.8x risk for type-1 diabetes | |
(G;G) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 133293192 |
Gene | FSTL4 |
is a | snp |
is | mentioned by |
dbSNP | rs17166496 |
dbSNP (classic) | rs17166496 |
ClinGen | rs17166496 |
ebi | rs17166496 |
HLI | rs17166496 |
Exac | rs17166496 |
Gnomad | rs17166496 |
Varsome | rs17166496 |
LitVar | rs17166496 |
Map | rs17166496 |
PheGenI | rs17166496 |
Biobank | rs17166496 |
1000 genomes | rs17166496 |
hgdp | rs17166496 |
ensembl | rs17166496 |
geneview | rs17166496 |
scholar | rs17166496 |
rs17166496 | |
pharmgkb | rs17166496 |
gwascentral | rs17166496 |
openSNP | rs17166496 |
23andMe | rs17166496 |
SNPshot | rs17166496 |
SNPdbe | rs17166496 |
MSV3d | rs17166496 |
GWAS Ctlg | rs17166496 |
GMAF | 0.4568 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
rs17166496 has been reported in a large study to be associated with type-1 diabetes.
The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 0.77 (CI 0.68-0.87), and for homozygotes, 1.09 (CI 0.92-1.29). [PMID 17554300]
Note: orientation of SNP is presumed correct but should be confirmed