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rs2186903

From SNPedia

Orientationplus
Stabilizedplus
Make rs2186903(A;A)
Make rs2186903(A;G)
Make rs2186903(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position107885825
is asnp
is mentioned by
dbSNPrs2186903
dbSNP (old)rs2186903
ClinGenrs2186903
ebirs2186903
HLIrs2186903
Exacrs2186903
Gnomadrs2186903
Varsomers2186903
Maprs2186903
PheGenIrs2186903
Biobankrs2186903
1000 genomesrs2186903
hgdprs2186903
ensemblrs2186903
gopubmedrs2186903
geneviewrs2186903
scholarrs2186903
googlers2186903
pharmgkbrs2186903
gwascentralrs2186903
openSNPrs2186903
23andMers2186903
23andMe allrs2186903
SNP Nexus

SNPshotrs2186903
SNPdbers2186903
MSV3drs2186903
GWAS Ctlgrs2186903
GMAF0.2544
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 4E-6
Odds Ratio 1.07 [1.04-1.11]