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

rs17043947

From SNPedia

Orientationplus
Stabilizedplus
Make rs17043947(C;C)
Make rs17043947(C;T)
Make rs17043947(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position22514115
is asnp
is mentioned by
dbSNPrs17043947
ebirs17043947
HLIrs17043947
Exacrs17043947
Varsomers17043947
Maprs17043947
PheGenIrs17043947
hapmaprs17043947
1000 genomesrs17043947
hgdprs17043947
ensemblrs17043947
gopubmedrs17043947
geneviewrs17043947
scholarrs17043947
googlers17043947
pharmgkbrs17043947
gwascentralrs17043947
openSNPrs17043947
23andMers17043947
23andMe allrs17043947
SNP Nexus

SNPshotrs17043947
SNPdbers17043947
MSV3drs17043947
GWAS Ctlgrs17043947
GMAF0.1102
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20707712OA-icon.png]
Trait
Title A genome-wide association study of self-rated health
Risk Allele T
P-val 2E-7
Odds Ratio 0.07 [NR] unit decrease