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rs2675399

From SNPedia

Orientationminus
Stabilizedminus
Make rs2675399(C;C)
Make rs2675399(C;T)
Make rs2675399(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position188854236
is asnp
is mentioned by
dbSNPrs2675399
ebirs2675399
HLIrs2675399
Exacrs2675399
Varsomers2675399
Maprs2675399
PheGenIrs2675399
hapmaprs2675399
1000 genomesrs2675399
hgdprs2675399
ensemblrs2675399
gopubmedrs2675399
geneviewrs2675399
scholarrs2675399
googlers2675399
pharmgkbrs2675399
gwascentralrs2675399
openSNPrs2675399
23andMers2675399
23andMe allrs2675399
SNP Nexus

SNPshotrs2675399
SNPdbers2675399
MSV3drs2675399
GWAS Ctlgrs2675399
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 6E-6
Odds Ratio .03 [NR] ng/mL increase