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rs7799006

From SNPedia

Orientationplus
Stabilizedplus
Make rs7799006(C;C)
Make rs7799006(C;T)
Make rs7799006(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position2238591
GeneMRM2
is asnp
is mentioned by
dbSNPrs7799006
dbSNP (classic)rs7799006
ClinGenrs7799006
ebirs7799006
HLIrs7799006
Exacrs7799006
Gnomadrs7799006
Varsomers7799006
LitVarrs7799006
Maprs7799006
PheGenIrs7799006
Biobankrs7799006
1000 genomesrs7799006
hgdprs7799006
ensemblrs7799006
geneviewrs7799006
scholarrs7799006
googlers7799006
pharmgkbrs7799006
gwascentralrs7799006
openSNPrs7799006
23andMers7799006
SNPshotrs7799006
SNPdbers7799006
MSV3drs7799006
GWAS Ctlgrs7799006
GMAF0.3682
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 C
P-val 5E-6
Odds Ratio 1.06 [1.03-1.08]