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

rs2058350

From SNPedia

Orientationplus
Stabilizedplus
Make rs2058350(C;C)
Make rs2058350(C;T)
Make rs2058350(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position3804261
is asnp
is mentioned by
dbSNPrs2058350
ebirs2058350
HLIrs2058350
Exacrs2058350
Varsomers2058350
Maprs2058350
PheGenIrs2058350
hapmaprs2058350
1000 genomesrs2058350
hgdprs2058350
ensemblrs2058350
gopubmedrs2058350
geneviewrs2058350
scholarrs2058350
googlers2058350
pharmgkbrs2058350
gwascentralrs2058350
openSNPrs2058350
23andMers2058350
23andMe allrs2058350
SNP Nexus

SNPshotrs2058350
SNPdbers2058350
MSV3drs2058350
GWAS Ctlgrs2058350
GMAF0.2906
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive performance
Title Common genetic variation and performance on standardized cognitive tests.
Risk Allele
P-val 8E-6
Odds Ratio NR NR