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rs490592

From SNPedia

Orientationminus
Stabilizedminus
Make rs490592(G;G)
Make rs490592(G;T)
Make rs490592(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116427650
is asnp
is mentioned by
dbSNPrs490592
ebirs490592
HLIrs490592
Exacrs490592
Varsomers490592
Maprs490592
PheGenIrs490592
hapmaprs490592
1000 genomesrs490592
hgdprs490592
ensemblrs490592
gopubmedrs490592
geneviewrs490592
scholarrs490592
googlers490592
pharmgkbrs490592
gwascentralrs490592
openSNPrs490592
23andMers490592
23andMe allrs490592
SNP Nexus

SNPshotrs490592
SNPdbers490592
MSV3drs490592
GWAS Ctlgrs490592
GMAF0.1791
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20171287OA-icon.png]
Trait Brain structure
Title Voxelwise Genome-Wide Association Study (vGWAS).
Risk Allele
P-val 0.000001
Odds Ratio None None