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rs12322695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common genotype
Make rs12322695(G;T)
Make rs12322695(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position116761609
GeneRNFT2
is asnp
is mentioned by
dbSNPrs12322695
dbSNP (classic)rs12322695
ClinGenrs12322695
ebirs12322695
HLIrs12322695
Exacrs12322695
Gnomadrs12322695
Varsomers12322695
LitVarrs12322695
Maprs12322695
PheGenIrs12322695
Biobankrs12322695
1000 genomesrs12322695
hgdprs12322695
ensemblrs12322695
geneviewrs12322695
scholarrs12322695
googlers12322695
pharmgkbrs12322695
gwascentralrs12322695
openSNPrs12322695
23andMers12322695
SNPshotrs12322695
SNPdbers12322695
MSV3drs12322695
GWAS Ctlgrs12322695
GMAF0.07713
Max Magnitude0
? (G;G) (G;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 7E-6
Odds Ratio .03 [NR] %awake time increase