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rs13361160

From SNPedia

Orientationplus
Stabilizedplus
Make rs13361160(C;C)
Make rs13361160(C;T)
Make rs13361160(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position10169711
is asnp
is mentioned by
dbSNPrs13361160
ebirs13361160
HLIrs13361160
Exacrs13361160
Varsomers13361160
Maprs13361160
PheGenIrs13361160
hapmaprs13361160
1000 genomesrs13361160
hgdprs13361160
ensemblrs13361160
gopubmedrs13361160
geneviewrs13361160
scholarrs13361160
googlers13361160
pharmgkbrs13361160
gwascentralrs13361160
openSNPrs13361160
23andMers13361160
23andMe allrs13361160
SNP Nexus

SNPshotrs13361160
SNPdbers13361160
MSV3drs13361160
GWAS Ctlgrs13361160
GMAF0.2704
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22956598OA-icon.png]
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]