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rs12871532

From SNPedia

Orientationplus
Stabilizedplus
Make rs12871532(C;C)
Make rs12871532(C;T)
Make rs12871532(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108016199
is asnp
is mentioned by
dbSNPrs12871532
dbSNP (classic)rs12871532
ClinGenrs12871532
ebirs12871532
HLIrs12871532
Exacrs12871532
Gnomadrs12871532
Varsomers12871532
LitVarrs12871532
Maprs12871532
PheGenIrs12871532
Biobankrs12871532
1000 genomesrs12871532
hgdprs12871532
ensemblrs12871532
geneviewrs12871532
scholarrs12871532
googlers12871532
pharmgkbrs12871532
gwascentralrs12871532
openSNPrs12871532
23andMers12871532
23andMe allrs12871532
SNPshotrs12871532
SNPdbers12871532
MSV3drs12871532
GWAS Ctlgrs12871532
GMAF0.4881
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 1E-6
Odds Ratio 1.06 [1.04-1.09]