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

rs6547705

From SNPedia

Orientationplus
Stabilizedplus
Make rs6547705(A;A)
Make rs6547705(A;G)
Make rs6547705(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position86817193
GeneCD8B
is asnp
is mentioned by
dbSNPrs6547705
ebirs6547705
HLIrs6547705
Exacrs6547705
Varsomers6547705
Maprs6547705
PheGenIrs6547705
hapmaprs6547705
1000 genomesrs6547705
hgdprs6547705
ensemblrs6547705
gopubmedrs6547705
geneviewrs6547705
scholarrs6547705
googlers6547705
pharmgkbrs6547705
gwascentralrs6547705
openSNPrs6547705
23andMers6547705
23andMe allrs6547705
SNP Nexus

SNPshotrs6547705
SNPdbers6547705
MSV3drs6547705
GWAS Ctlgrs6547705
GMAF0.1253
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21685912OA-icon.png]
Trait
Title Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Risk Allele
P-val 1E-8
Odds Ratio 1.2800 [1.18-1.40]