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

rs2567426

From SNPedia

Orientationminus
Stabilizedminus
Make rs2567426(C;C)
Make rs2567426(C;T)
Make rs2567426(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position95789632
is asnp
is mentioned by
dbSNPrs2567426
dbSNP (classic)rs2567426
ClinGenrs2567426
ebirs2567426
HLIrs2567426
Exacrs2567426
Gnomadrs2567426
Varsomers2567426
LitVarrs2567426
Maprs2567426
PheGenIrs2567426
Biobankrs2567426
1000 genomesrs2567426
hgdprs2567426
ensemblrs2567426
geneviewrs2567426
scholarrs2567426
googlers2567426
pharmgkbrs2567426
gwascentralrs2567426
openSNPrs2567426
23andMers2567426
SNPshotrs2567426
SNPdbers2567426
MSV3drs2567426
GWAS Ctlgrs2567426
GMAF0.2617
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21130836OA-icon.png]
Trait
Title Whole genome association scan for genetic polymorphisms influencing information processing speed
Risk Allele A
P-val 0.000003
Odds Ratio 0.1300 [0.07-0.19] unit increase