rs12901001
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12901001(A;A) |
Make rs12901001(A;G) |
Make rs12901001(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 86316245 |
Gene | AGBL1, AGBL1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs12901001 |
dbSNP (classic) | rs12901001 |
ClinGen | rs12901001 |
ebi | rs12901001 |
HLI | rs12901001 |
Exac | rs12901001 |
Gnomad | rs12901001 |
Varsome | rs12901001 |
LitVar | rs12901001 |
Map | rs12901001 |
PheGenI | rs12901001 |
Biobank | rs12901001 |
1000 genomes | rs12901001 |
hgdp | rs12901001 |
ensembl | rs12901001 |
geneview | rs12901001 |
scholar | rs12901001 |
rs12901001 | |
pharmgkb | rs12901001 |
gwascentral | rs12901001 |
openSNP | rs12901001 |
23andMe | rs12901001 |
SNPshot | rs12901001 |
SNPdbe | rs12901001 |
MSV3d | rs12901001 |
GWAS Ctlg | rs12901001 |
GMAF | 0.461 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22961001] |
Trait | Barrett's esophagus |
Title | Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. |
Risk Allele | |
P-val | 6E-6 |
Odds Ratio | .15 [0.091-0.209] unit increase |