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

rs13169113

From SNPedia

Orientationplus
Stabilizedplus
Make rs13169113(A;A)
Make rs13169113(A;C)
Make rs13169113(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position126002782
is asnp
is mentioned by
dbSNPrs13169113
ebirs13169113
HLIrs13169113
Exacrs13169113
Varsomers13169113
Maprs13169113
PheGenIrs13169113
hapmaprs13169113
1000 genomesrs13169113
hgdprs13169113
ensemblrs13169113
gopubmedrs13169113
geneviewrs13169113
scholarrs13169113
googlers13169113
pharmgkbrs13169113
gwascentralrs13169113
openSNPrs13169113
23andMers13169113
23andMe allrs13169113
SNP Nexus

SNPshotrs13169113
SNPdbers13169113
MSV3drs13169113
GWAS Ctlgrs13169113
GMAF0.3898
Max Magnitude
? (A;A) (A;C) (C;C) 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 9E-6
Odds Ratio NR NR