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rs6075982

From SNPedia

Orientationplus
Stabilizedplus
Make rs6075982(C;C)
Make rs6075982(C;T)
Make rs6075982(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position22906619
is asnp
is mentioned by
dbSNPrs6075982
ebirs6075982
HLIrs6075982
Exacrs6075982
Varsomers6075982
Maprs6075982
PheGenIrs6075982
hapmaprs6075982
1000 genomesrs6075982
hgdprs6075982
ensemblrs6075982
gopubmedrs6075982
geneviewrs6075982
scholarrs6075982
googlers6075982
pharmgkbrs6075982
gwascentralrs6075982
openSNPrs6075982
23andMers6075982
23andMe allrs6075982
SNP Nexus

SNPshotrs6075982
SNPdbers6075982
MSV3drs6075982
GWAS Ctlgrs6075982
GMAF0.3159
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 3E-6
Odds Ratio .04 [NR] g/d increase