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rs12408810

From SNPedia

Orientationplus
Stabilizedplus
Make rs12408810(C;C)
Make rs12408810(C;T)
Make rs12408810(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position106098321
is asnp
is mentioned by
dbSNPrs12408810
ebirs12408810
HLIrs12408810
Exacrs12408810
Varsomers12408810
Maprs12408810
PheGenIrs12408810
hapmaprs12408810
1000 genomesrs12408810
hgdprs12408810
ensemblrs12408810
gopubmedrs12408810
geneviewrs12408810
scholarrs12408810
googlers12408810
pharmgkbrs12408810
gwascentralrs12408810
openSNPrs12408810
23andMers12408810
23andMe allrs12408810
SNP Nexus

SNPshotrs12408810
SNPdbers12408810
MSV3drs12408810
GWAS Ctlgrs12408810
GMAF0.2599
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23563609OA-icon.png]
Trait Obesity (early onset extreme)
Title Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Risk Allele C
P-val 9E-6
Odds Ratio 1.25 [1.13-1.38]