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

rs7782376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7782376(A;A)
Make rs7782376(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position116937070
is asnp
is mentioned by
dbSNPrs7782376
ebirs7782376
HLIrs7782376
Exacrs7782376
Varsomers7782376
Maprs7782376
PheGenIrs7782376
hapmaprs7782376
1000 genomesrs7782376
hgdprs7782376
ensemblrs7782376
gopubmedrs7782376
geneviewrs7782376
scholarrs7782376
googlers7782376
pharmgkbrs7782376
gwascentralrs7782376
openSNPrs7782376
23andMers7782376
23andMe allrs7782376
SNP Nexus

SNPshotrs7782376
SNPdbers7782376
MSV3drs7782376
GWAS Ctlgrs7782376
GMAF0.3747
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 8 x 10^-6) for forward digit span
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