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rs9491640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9491640(A;A)
Make rs9491640(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position98471388
is asnp
is mentioned by
dbSNPrs9491640
ebirs9491640
HLIrs9491640
Exacrs9491640
Varsomers9491640
Maprs9491640
PheGenIrs9491640
hapmaprs9491640
1000 genomesrs9491640
hgdprs9491640
ensemblrs9491640
gopubmedrs9491640
geneviewrs9491640
scholarrs9491640
googlers9491640
pharmgkbrs9491640
gwascentralrs9491640
openSNPrs9491640
23andMers9491640
23andMe allrs9491640
SNP Nexus

SNPshotrs9491640
SNPdbers9491640
MSV3drs9491640
GWAS Ctlgrs9491640
GMAF0.04545
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19023125OA-icon.png]
Trait Brain imaging in schizophrenia (interaction)
Title A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype
Risk Allele
P-val 0.000009
Odds Ratio NR NR



GET Evidence
rs9491640
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.046875
summary