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rs1795708

From SNPedia

Orientationplus
Stabilizedplus
Make rs1795708(C;C)
Make rs1795708(C;T)
Make rs1795708(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position58356897
is asnp
is mentioned by
dbSNPrs1795708
ebirs1795708
HLIrs1795708
Exacrs1795708
Varsomers1795708
Maprs1795708
PheGenIrs1795708
hapmaprs1795708
1000 genomesrs1795708
hgdprs1795708
ensemblrs1795708
gopubmedrs1795708
geneviewrs1795708
scholarrs1795708
googlers1795708
pharmgkbrs1795708
gwascentralrs1795708
openSNPrs1795708
23andMers1795708
23andMe allrs1795708
SNP Nexus

SNPshotrs1795708
SNPdbers1795708
MSV3drs1795708
GWAS Ctlgrs1795708
GMAF0.3163
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 G
P-val 4E-6
Odds Ratio .04 [NR] g/d increase