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

rs7841189

From SNPedia

Orientationplus
Stabilizedplus
Make rs7841189(C;C)
Make rs7841189(C;T)
Make rs7841189(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position19987865
is asnp
is mentioned by
dbSNPrs7841189
ebirs7841189
HLIrs7841189
Exacrs7841189
Varsomers7841189
Maprs7841189
PheGenIrs7841189
hapmaprs7841189
1000 genomesrs7841189
hgdprs7841189
ensemblrs7841189
gopubmedrs7841189
geneviewrs7841189
scholarrs7841189
googlers7841189
pharmgkbrs7841189
gwascentralrs7841189
openSNPrs7841189
23andMers7841189
23andMe allrs7841189
SNP Nexus

SNPshotrs7841189
SNPdbers7841189
MSV3drs7841189
GWAS Ctlgrs7841189
GMAF0.1488
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-14
Odds Ratio 0.1800 None