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rs9951602

From SNPedia

Orientationplus
Stabilizedplus
Make rs9951602(C;C)
Make rs9951602(C;T)
Make rs9951602(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position78897779
is asnp
is mentioned by
dbSNPrs9951602
ebirs9951602
HLIrs9951602
Exacrs9951602
Varsomers9951602
Maprs9951602
PheGenIrs9951602
hapmaprs9951602
1000 genomesrs9951602
hgdprs9951602
ensemblrs9951602
gopubmedrs9951602
geneviewrs9951602
scholarrs9951602
googlers9951602
pharmgkbrs9951602
gwascentralrs9951602
openSNPrs9951602
23andMers9951602
23andMe allrs9951602
SNP Nexus

SNPshotrs9951602
SNPdbers9951602
MSV3drs9951602
GWAS Ctlgrs9951602
GMAF0.2117
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23251661OA-icon.png]
Trait Obesity-related traits
Title Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele A
P-val 9E-6
Odds Ratio .03 [NR] ng/mL increase


[PMID 18372901OA-icon.png] Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.