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rs7659062

From SNPedia

Orientationplus
Stabilizedplus
Make rs7659062(C;C)
Make rs7659062(C;T)
Make rs7659062(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position188665925
is asnp
is mentioned by
dbSNPrs7659062
ebirs7659062
HLIrs7659062
Exacrs7659062
Varsomers7659062
Maprs7659062
PheGenIrs7659062
hapmaprs7659062
1000 genomesrs7659062
hgdprs7659062
ensemblrs7659062
gopubmedrs7659062
geneviewrs7659062
scholarrs7659062
googlers7659062
pharmgkbrs7659062
gwascentralrs7659062
openSNPrs7659062
23andMers7659062
23andMe allrs7659062
SNP Nexus

SNPshotrs7659062
SNPdbers7659062
MSV3drs7659062
GWAS Ctlgrs7659062
GMAF0.1377
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 8 x 10^-6) - Delayed Story Recall
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000008
Odds Ratio None None