Have questions? Visit https://www.reddit.com/r/SNPedia

rs6711016

From SNPedia

Orientationplus
Stabilizedplus
Make rs6711016(A;A)
Make rs6711016(A;C)
Make rs6711016(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position20923592
is asnp
is mentioned by
dbSNPrs6711016
ebirs6711016
HLIrs6711016
Exacrs6711016
Varsomers6711016
Maprs6711016
PheGenIrs6711016
hapmaprs6711016
1000 genomesrs6711016
hgdprs6711016
ensemblrs6711016
gopubmedrs6711016
geneviewrs6711016
scholarrs6711016
googlers6711016
pharmgkbrs6711016
gwascentralrs6711016
openSNPrs6711016
23andMers6711016
23andMe allrs6711016
SNP Nexus

SNPshotrs6711016
SNPdbers6711016
MSV3drs6711016
GWAS Ctlgrs6711016
GMAF0.2815
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22399527OA-icon.png]
Trait
Title Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
Risk Allele C
P-val 4E-8
Odds Ratio 0.0800 None