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rs6961611

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6961611(C;C)
Make rs6961611(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position67961336
is asnp
is mentioned by
dbSNPrs6961611
ebirs6961611
HLIrs6961611
Exacrs6961611
Varsomers6961611
Maprs6961611
PheGenIrs6961611
hapmaprs6961611
1000 genomesrs6961611
hgdprs6961611
ensemblrs6961611
gopubmedrs6961611
geneviewrs6961611
scholarrs6961611
googlers6961611
pharmgkbrs6961611
gwascentralrs6961611
openSNPrs6961611
23andMers6961611
23andMe allrs6961611
SNP Nexus

SNPshotrs6961611
SNPdbers6961611
MSV3drs6961611
GWAS Ctlgrs6961611
GMAF0.08953
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21130836OA-icon.png]
Trait
Title Whole genome association scan for genetic polymorphisms influencing information processing speed
Risk Allele T
P-val 0.000007
Odds Ratio 0.6300 [0.36-0.90] unit decrease