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rs7849973

From SNPedia

Orientationplus
Stabilizedplus
Make rs7849973(C;C)
Make rs7849973(C;G)
Make rs7849973(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position22819577
GeneLINC01239
is asnp
is mentioned by
dbSNPrs7849973
dbSNP (classic)rs7849973
ClinGenrs7849973
ebirs7849973
HLIrs7849973
Exacrs7849973
Gnomadrs7849973
Varsomers7849973
LitVarrs7849973
Maprs7849973
PheGenIrs7849973
Biobankrs7849973
1000 genomesrs7849973
hgdprs7849973
ensemblrs7849973
geneviewrs7849973
scholarrs7849973
googlers7849973
pharmgkbrs7849973
gwascentralrs7849973
openSNPrs7849973
23andMers7849973
SNPshotrs7849973
SNPdbers7849973
MSV3drs7849973
GWAS Ctlgrs7849973
GMAF0.2759
Max Magnitude0
? (C;C) (C;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
P-val 8E-6
Odds Ratio 1.05 [1.02-1.08]