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rs11212364

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11212364(A;G)
Make rs11212364(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position97703984
is asnp
is mentioned by
dbSNPrs11212364
dbSNP (classic)rs11212364
ClinGenrs11212364
ebirs11212364
HLIrs11212364
Exacrs11212364
Gnomadrs11212364
Varsomers11212364
LitVarrs11212364
Maprs11212364
PheGenIrs11212364
Biobankrs11212364
1000 genomesrs11212364
hgdprs11212364
ensemblrs11212364
geneviewrs11212364
scholarrs11212364
googlers11212364
pharmgkbrs11212364
gwascentralrs11212364
openSNPrs11212364
23andMers11212364
SNPshotrs11212364
SNPdbers11212364
MSV3drs11212364
GWAS Ctlgrs11212364
GMAF0.06703
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.2600 [0.16-0.36] unit decrease