rs3087879
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs3087879(C;C) |
Make rs3087879(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 4586808 |
Gene | SLC1A1, SPATA6L |
is a | snp |
is | mentioned by |
dbSNP | rs3087879 |
dbSNP (classic) | rs3087879 |
ClinGen | rs3087879 |
ebi | rs3087879 |
HLI | rs3087879 |
Exac | rs3087879 |
Gnomad | rs3087879 |
Varsome | rs3087879 |
LitVar | rs3087879 |
Map | rs3087879 |
PheGenI | rs3087879 |
Biobank | rs3087879 |
1000 genomes | rs3087879 |
hgdp | rs3087879 |
ensembl | rs3087879 |
geneview | rs3087879 |
scholar | rs3087879 |
rs3087879 | |
pharmgkb | rs3087879 |
gwascentral | rs3087879 |
openSNP | rs3087879 |
23andMe | rs3087879 |
SNPshot | rs3087879 |
SNPdbe | rs3087879 |
MSV3d | rs3087879 |
GWAS Ctlg | rs3087879 |
GMAF | 0.2374 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 19349310] A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder
[PMID 22665263] Molecular genetics of obsessive-compulsive disorder: a comprehensive meta-analysis of genetic association studies
[PMID 19324536] Glutamate receptor gene (GRIN2B) associated with reduced anterior cingulate glutamatergic concentration in pediatric obsessive-compulsive disorder.
[PMID 22776887] Interaction of SLC1A1 gene variants and life stress on pharmacological resistance in obsessive-compulsive disorder.
[PMID 26254621] Association between genetic variants related to glutamatergic, dopaminergic and neurodevelopment pathways and white matter microstructure in child and adolescent patients with obsessive-compulsive disorder
ClinVar | |
---|---|
Risk | rs3087879(C;C) |
Alt | rs3087879(C;C) |
Reference | Rs3087879(G;G) |
Significance | Non-pathogenic |
Disease | Dicarboxylic aminoaciduria |
Variation | info |
Gene | SPATA6L SLC1A1 |
CLNDBN | Dicarboxylic aminoaciduria |
Reversed | 0 |
HGVS | NC_000009.11:g.4586808G>C |
CLNSRC | |
CLNACC | RCV000273817.1, |