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rs10873998

From SNPedia

Orientationplus
Stabilizedplus
Make rs10873998(C;C)
Make rs10873998(C;T)
Make rs10873998(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position78798120
is asnp
is mentioned by
dbSNPrs10873998
dbSNP (classic)rs10873998
ClinGenrs10873998
ebirs10873998
HLIrs10873998
Exacrs10873998
Gnomadrs10873998
Varsomers10873998
LitVarrs10873998
Maprs10873998
PheGenIrs10873998
Biobankrs10873998
1000 genomesrs10873998
hgdprs10873998
ensemblrs10873998
geneviewrs10873998
scholarrs10873998
googlers10873998
pharmgkbrs10873998
gwascentralrs10873998
openSNPrs10873998
23andMers10873998
23andMe allrs10873998
SNPshotrs10873998
SNPdbers10873998
MSV3drs10873998
GWAS Ctlgrs10873998
GMAF0.4596
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 4E-6
Odds Ratio 1.06 [1.03-1.09]