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rs7873102

From SNPedia

Orientationplus
Stabilizedplus
Make rs7873102(G;G)
Make rs7873102(G;T)
Make rs7873102(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position38041145
GeneSHB
is asnp
is mentioned by
dbSNPrs7873102
ebirs7873102
HLIrs7873102
Exacrs7873102
Varsomers7873102
Maprs7873102
PheGenIrs7873102
hapmaprs7873102
1000 genomesrs7873102
hgdprs7873102
ensemblrs7873102
gopubmedrs7873102
geneviewrs7873102
scholarrs7873102
googlers7873102
pharmgkbrs7873102
gwascentralrs7873102
openSNPrs7873102
23andMers7873102
23andMe allrs7873102
SNP Nexus

SNPshotrs7873102
SNPdbers7873102
MSV3drs7873102
GWAS Ctlgrs7873102
GMAF0.4807
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 6E-7
Odds Ratio None None