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rs5951698

From SNPedia

Orientationplus
Stabilizedplus
Make rs5951698(A;A)
Make rs5951698(A;G)
Make rs5951698(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position22116540
GenePHEX
is asnp
is mentioned by
dbSNPrs5951698
ebirs5951698
HLIrs5951698
Exacrs5951698
Varsomers5951698
Maprs5951698
PheGenIrs5951698
hapmaprs5951698
1000 genomesrs5951698
hgdprs5951698
ensemblrs5951698
gopubmedrs5951698
geneviewrs5951698
scholarrs5951698
googlers5951698
pharmgkbrs5951698
gwascentralrs5951698
openSNPrs5951698
23andMers5951698
23andMe allrs5951698
SNP Nexus

SNPshotrs5951698
SNPdbers5951698
MSV3drs5951698
GWAS Ctlgrs5951698
GMAF0.1372
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 6E-6
Odds Ratio 5.65 [NR]