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rs7948661

From SNPedia

Orientationplus
Stabilizedplus
Make rs7948661(C;C)
Make rs7948661(C;T)
Make rs7948661(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position118470934
GeneMLL
is asnp
is mentioned by
dbSNPrs7948661
ebirs7948661
HLIrs7948661
Exacrs7948661
Varsomers7948661
Maprs7948661
PheGenIrs7948661
hapmaprs7948661
1000 genomesrs7948661
hgdprs7948661
ensemblrs7948661
gopubmedrs7948661
geneviewrs7948661
scholarrs7948661
googlers7948661
pharmgkbrs7948661
gwascentralrs7948661
openSNPrs7948661
23andMers7948661
23andMe allrs7948661
SNP Nexus

SNPshotrs7948661
SNPdbers7948661
MSV3drs7948661
GWAS Ctlgrs7948661
GMAF0.06061
Max Magnitude
? (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 1.05 [1.00-1.10]