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rs10250997

From SNPedia

Orientationplus
Stabilizedplus
Make rs10250997(A;A)
Make rs10250997(A;C)
Make rs10250997(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position136461788
is asnp
is mentioned by
dbSNPrs10250997
dbSNP (classic)rs10250997
ClinGenrs10250997
ebirs10250997
HLIrs10250997
Exacrs10250997
Gnomadrs10250997
Varsomers10250997
LitVarrs10250997
Maprs10250997
PheGenIrs10250997
Biobankrs10250997
1000 genomesrs10250997
hgdprs10250997
ensemblrs10250997
geneviewrs10250997
scholarrs10250997
googlers10250997
pharmgkbrs10250997
gwascentralrs10250997
openSNPrs10250997
23andMers10250997
23andMe allrs10250997
SNPshotrs10250997
SNPdbers10250997
MSV3drs10250997
GWAS Ctlgrs10250997
GMAF0.09871
Max Magnitude0
? (A;A) (A;C) (C;C) 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 8E-6
Odds Ratio 1.03 [0.99-1.07]