rs10491734
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1.4x risk of early onset OCD | |
(A;G) | 1.4x risk of early onset OCD | |
(G;G) | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 4482706 |
is a | snp |
is | mentioned by |
dbSNP | rs10491734 |
dbSNP (classic) | rs10491734 |
ClinGen | rs10491734 |
ebi | rs10491734 |
HLI | rs10491734 |
Exac | rs10491734 |
Gnomad | rs10491734 |
Varsome | rs10491734 |
LitVar | rs10491734 |
Map | rs10491734 |
PheGenI | rs10491734 |
Biobank | rs10491734 |
1000 genomes | rs10491734 |
hgdp | rs10491734 |
ensembl | rs10491734 |
geneview | rs10491734 |
scholar | rs10491734 |
rs10491734 | |
pharmgkb | rs10491734 |
gwascentral | rs10491734 |
openSNP | rs10491734 |
23andMe | rs10491734 |
SNPshot | rs10491734 |
SNPdbe | rs10491734 |
MSV3d | rs10491734 |
GWAS Ctlg | rs10491734 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23411042] Association of the candidate gene SLC1A1 and obsessive-compulsive disorder in Han Chinese population