rs348594
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs348594(A;A) |
Make rs348594(A;G) |
Make rs348594(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 40323836 |
Gene | LOC105374736 |
is a | snp |
is | mentioned by |
dbSNP | rs348594 |
dbSNP (classic) | rs348594 |
ClinGen | rs348594 |
ebi | rs348594 |
HLI | rs348594 |
Exac | rs348594 |
Gnomad | rs348594 |
Varsome | rs348594 |
LitVar | rs348594 |
Map | rs348594 |
PheGenI | rs348594 |
Biobank | rs348594 |
1000 genomes | rs348594 |
hgdp | rs348594 |
ensembl | rs348594 |
geneview | rs348594 |
scholar | rs348594 |
rs348594 | |
pharmgkb | rs348594 |
gwascentral | rs348594 |
openSNP | rs348594 |
23andMe | rs348594 |
SNPshot | rs348594 |
SNPdbe | rs348594 |
MSV3d | rs348594 |
GWAS Ctlg | rs348594 |
GMAF | 0.4917 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Rs348594 | |
---|---|
PubMed | [PMID 17447842] |
Affy Probeset | SNP_A-8391321 |
Affy Orientation | same |
On GW 5.0 | 0 |
Alleles A/B | A/G |
Ancestral | G |
Population | EU |
Allele | A |
Case Freq. | 0.67 |
Control Freq. | 0.6 |
Odds Ratio Het | |
Odds Ratio Hom | |
Odds Ratio All | 1.36 |
Disease | Crohn's disease (CD) |
rs348594 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele [PMID 17447842]