Have questions? Visit https://www.reddit.com/r/SNPedia

rs769111

From SNPedia

Orientationminus
Stabilizedminus
Make rs769111(A;A)
Make rs769111(A;C)
Make rs769111(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position12020180
is asnp
is mentioned by
dbSNPrs769111
ebirs769111
HLIrs769111
Exacrs769111
Varsomers769111
Maprs769111
PheGenIrs769111
hapmaprs769111
1000 genomesrs769111
hgdprs769111
ensemblrs769111
gopubmedrs769111
geneviewrs769111
scholarrs769111
googlers769111
pharmgkbrs769111
gwascentralrs769111
openSNPrs769111
23andMers769111
23andMe allrs769111
SNP Nexus

SNPshotrs769111
SNPdbers769111
MSV3drs769111
GWAS Ctlgrs769111
GMAF0.4109
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22889924OA-icon.png]
Trait Tourette syndrome
Title Genome-wide association study of Tourette's syndrome.
Risk Allele T
P-val 6E-6
Odds Ratio 1.23 [NR]