rs5951698
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common genotype |
Make rs5951698(A;G) |
Make rs5951698(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 22116540 |
Gene | PHEX |
is a | snp |
is | mentioned by |
dbSNP | rs5951698 |
dbSNP (classic) | rs5951698 |
ClinGen | rs5951698 |
ebi | rs5951698 |
HLI | rs5951698 |
Exac | rs5951698 |
Gnomad | rs5951698 |
Varsome | rs5951698 |
LitVar | rs5951698 |
Map | rs5951698 |
PheGenI | rs5951698 |
Biobank | rs5951698 |
1000 genomes | rs5951698 |
hgdp | rs5951698 |
ensembl | rs5951698 |
geneview | rs5951698 |
scholar | rs5951698 |
rs5951698 | |
pharmgkb | rs5951698 |
gwascentral | rs5951698 |
openSNP | rs5951698 |
23andMe | rs5951698 |
SNPshot | rs5951698 |
SNPdbe | rs5951698 |
MSV3d | rs5951698 |
GWAS Ctlg | rs5951698 |
GMAF | 0.1372 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22889924] |
Trait | Tourette syndrome |
Title | Genome-wide association study of Tourette's syndrome. |
Risk Allele | G |
P-val | 6E-6 |
Odds Ratio | 5.65 [NR] |