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rs7565792

From SNPedia

Orientationplus
Stabilizedplus
Make rs7565792(C;C)
Make rs7565792(C;T)
Make rs7565792(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position48422566
is asnp
is mentioned by
dbSNPrs7565792
ebirs7565792
HLIrs7565792
Exacrs7565792
Varsomers7565792
Maprs7565792
PheGenIrs7565792
hapmaprs7565792
1000 genomesrs7565792
hgdprs7565792
ensemblrs7565792
gopubmedrs7565792
geneviewrs7565792
scholarrs7565792
googlers7565792
pharmgkbrs7565792
gwascentralrs7565792
openSNPrs7565792
23andMers7565792
23andMe allrs7565792
SNP Nexus

SNPshotrs7565792
SNPdbers7565792
MSV3drs7565792
GWAS Ctlgrs7565792
GMAF0.4624
Max Magnitude
? (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 C
P-val 7E-6
Odds Ratio 1.03 [1.00-1.06]