rs13361160
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13361160(C;C) |
Make rs13361160(C;T) |
Make rs13361160(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 10169711 |
is a | snp |
is | mentioned by |
dbSNP | rs13361160 |
dbSNP (classic) | rs13361160 |
ClinGen | rs13361160 |
ebi | rs13361160 |
HLI | rs13361160 |
Exac | rs13361160 |
Gnomad | rs13361160 |
Varsome | rs13361160 |
LitVar | rs13361160 |
Map | rs13361160 |
PheGenI | rs13361160 |
Biobank | rs13361160 |
1000 genomes | rs13361160 |
hgdp | rs13361160 |
ensembl | rs13361160 |
geneview | rs13361160 |
scholar | rs13361160 |
rs13361160 | |
pharmgkb | rs13361160 |
gwascentral | rs13361160 |
openSNP | rs13361160 |
23andMe | rs13361160 |
SNPshot | rs13361160 |
SNPdbe | rs13361160 |
MSV3d | rs13361160 |
GWAS Ctlg | rs13361160 |
GMAF | 0.2704 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22956598] |
Trait | Pain |
Title | Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. |
Risk Allele | C |
P-val | 5E-7 |
Odds Ratio | 1.17 [1.10-1.24] |