rs10990268
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10990268(C;C) |
Make rs10990268(C;T) |
Make rs10990268(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 102740216 |
is a | snp |
is | mentioned by |
dbSNP | rs10990268 |
dbSNP (classic) | rs10990268 |
ClinGen | rs10990268 |
ebi | rs10990268 |
HLI | rs10990268 |
Exac | rs10990268 |
Gnomad | rs10990268 |
Varsome | rs10990268 |
LitVar | rs10990268 |
Map | rs10990268 |
PheGenI | rs10990268 |
Biobank | rs10990268 |
1000 genomes | rs10990268 |
hgdp | rs10990268 |
ensembl | rs10990268 |
geneview | rs10990268 |
scholar | rs10990268 |
rs10990268 | |
pharmgkb | rs10990268 |
gwascentral | rs10990268 |
openSNP | rs10990268 |
23andMe | rs10990268 |
SNPshot | rs10990268 |
SNPdbe | rs10990268 |
MSV3d | rs10990268 |
GWAS Ctlg | rs10990268 |
GMAF | 0.1951 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22889924![]() |
Trait | Tourette syndrome |
Title | Genome-wide association study of Tourette's syndrome. |
Risk Allele | C |
P-val | 5E-6 |
Odds Ratio | 1.29 [NR] |