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rs7868992

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1.29x risk of Tourette's Syndrome
(A;G) 1.29x risk of Tourette's Syndrome
(G;G) normal
ReferenceGRCh38 38.1/141
Chromosome9
Position114228791
GeneCOL27A1
is asnp
is mentioned by
dbSNPrs7868992
ebirs7868992
HLIrs7868992
Exacrs7868992
Varsomers7868992
Maprs7868992
PheGenIrs7868992
hapmaprs7868992
1000 genomesrs7868992
hgdprs7868992
ensemblrs7868992
gopubmedrs7868992
geneviewrs7868992
scholarrs7868992
googlers7868992
pharmgkbrs7868992
gwascentralrs7868992
openSNPrs7868992
23andMers7868992
23andMe allrs7868992
SNP Nexus

SNPshotrs7868992
SNPdbers7868992
MSV3drs7868992
GWAS Ctlgrs7868992
GMAF0.4582
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22889924OA-icon.png]
Trait Tourette syndrome
Title Genome-wide association study of Tourette's syndrome.
Risk Allele G
P-val 3E-8
Odds Ratio 1.29 [NR]