rs2342002
From SNPedia
Orientation | plus |
Stabilized | minus |
Make rs2342002(C;C) |
Make rs2342002(C;T) |
Make rs2342002(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 61285855 |
is a | snp |
is | mentioned by |
dbSNP | rs2342002 |
dbSNP (classic) | rs2342002 |
ClinGen | rs2342002 |
ebi | rs2342002 |
HLI | rs2342002 |
Exac | rs2342002 |
Gnomad | rs2342002 |
Varsome | rs2342002 |
LitVar | rs2342002 |
Map | rs2342002 |
PheGenI | rs2342002 |
Biobank | rs2342002 |
1000 genomes | rs2342002 |
hgdp | rs2342002 |
ensembl | rs2342002 |
geneview | rs2342002 |
scholar | rs2342002 |
rs2342002 | |
pharmgkb | rs2342002 |
gwascentral | rs2342002 |
openSNP | rs2342002 |
23andMe | rs2342002 |
SNPshot | rs2342002 |
SNPdbe | rs2342002 |
MSV3d | rs2342002 |
GWAS Ctlg | rs2342002 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24121790] |
Trait | Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) |
Title | A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. |
Risk Allele | T |
P-val | 7E-6 |
Odds Ratio | 1.15 [1.08-1.23] |