rs2145418
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 2.5 | 9.2x increased thyroid cancer risk |
(G;T) | 2.2 | 5.0x increased thyroid cancer risk |
(T;T) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 118422631 |
is a | snp |
is | mentioned by |
dbSNP | rs2145418 |
dbSNP (classic) | rs2145418 |
ClinGen | rs2145418 |
ebi | rs2145418 |
HLI | rs2145418 |
Exac | rs2145418 |
Gnomad | rs2145418 |
Varsome | rs2145418 |
LitVar | rs2145418 |
Map | rs2145418 |
PheGenI | rs2145418 |
Biobank | rs2145418 |
1000 genomes | rs2145418 |
hgdp | rs2145418 |
ensembl | rs2145418 |
geneview | rs2145418 |
scholar | rs2145418 |
rs2145418 | |
pharmgkb | rs2145418 |
gwascentral | rs2145418 |
openSNP | rs2145418 |
23andMe | rs2145418 |
SNPshot | rs2145418 |
SNPdbe | rs2145418 |
MSV3d | rs2145418 |
GWAS Ctlg | rs2145418 |
GMAF | 0.2557 |
Max Magnitude | 2.5 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
rs2145418 is a SNP in the chromosome 1p12-13 region.
In a case-control association study in a Spanish population, rs2145418 was associated with increased risk for thyroid cancer. rs2145418(G;T) heterozygotes had an odds ratio of 5.0 (CI: 2.85 - 8.83), while (G;G) homozygotes had an increased odds ratio of 9.2 (CI: 4.50 - 21.6), with reported significance of p < 0.0001.[PMID 18559567]