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

rs3784962

From SNPedia

Orientationplus
Stabilizedplus
Make rs3784962(A;A)
Make rs3784962(A;G)
Make rs3784962(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position83723723
GeneCDH13
is asnp
is mentioned by
dbSNPrs3784962
ebirs3784962
HLIrs3784962
Exacrs3784962
Varsomers3784962
Maprs3784962
PheGenIrs3784962
hapmaprs3784962
1000 genomesrs3784962
hgdprs3784962
ensemblrs3784962
gopubmedrs3784962
geneviewrs3784962
scholarrs3784962
googlers3784962
pharmgkbrs3784962
gwascentralrs3784962
openSNPrs3784962
23andMers3784962
23andMe allrs3784962
SNP Nexus

SNPshotrs3784962
SNPdbers3784962
MSV3drs3784962
GWAS Ctlgrs3784962
GMAF0.3673
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 3 x 10^-6) for Trails B performance
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000003
Odds Ratio None None