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rs6602217

From SNPedia

Orientationplus
Stabilizedplus
Make rs6602217(C;C)
Make rs6602217(C;T)
Make rs6602217(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position6904301
GeneLOC105376387
is asnp
is mentioned by
dbSNPrs6602217
dbSNP (classic)rs6602217
ClinGenrs6602217
ebirs6602217
HLIrs6602217
Exacrs6602217
Gnomadrs6602217
Varsomers6602217
LitVarrs6602217
Maprs6602217
PheGenIrs6602217
Biobankrs6602217
1000 genomesrs6602217
hgdprs6602217
ensemblrs6602217
geneviewrs6602217
scholarrs6602217
googlers6602217
pharmgkbrs6602217
gwascentralrs6602217
openSNPrs6602217
23andMers6602217
SNPshotrs6602217
SNPdbers6602217
MSV3drs6602217
GWAS Ctlgrs6602217
GMAF0.1203
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 2E-6
Odds Ratio 1.12 [1.07-1.17]