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

rs9951150

From SNPedia

Orientationplus
Stabilizedplus
Make rs9951150(A;A)
Make rs9951150(A;G)
Make rs9951150(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position55153893
is asnp
is mentioned by
dbSNPrs9951150
dbSNP (old)rs9951150
ClinGenrs9951150
ebirs9951150
HLIrs9951150
Exacrs9951150
Gnomadrs9951150
Varsomers9951150
Maprs9951150
PheGenIrs9951150
Biobankrs9951150
1000 genomesrs9951150
hgdprs9951150
ensemblrs9951150
gopubmedrs9951150
geneviewrs9951150
scholarrs9951150
googlers9951150
pharmgkbrs9951150
gwascentralrs9951150
openSNPrs9951150
23andMers9951150
23andMe allrs9951150
SNP Nexus

SNPshotrs9951150
SNPdbers9951150
MSV3drs9951150
GWAS Ctlgrs9951150
GMAF0.4798
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23453885OA-icon.png]
Trait Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele A
P-val 6E-7
Odds Ratio 1.06 [1.04-1.09]