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rs3087879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3087879(C;C)
Make rs3087879(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position4586808
GeneSLC1A1, SPATA6L
is asnp
is mentioned by
dbSNPrs3087879
dbSNP (classic)rs3087879
ClinGenrs3087879
ebirs3087879
HLIrs3087879
Exacrs3087879
Gnomadrs3087879
Varsomers3087879
LitVarrs3087879
Maprs3087879
PheGenIrs3087879
Biobankrs3087879
1000 genomesrs3087879
hgdprs3087879
ensemblrs3087879
geneviewrs3087879
scholarrs3087879
googlers3087879
pharmgkbrs3087879
gwascentralrs3087879
openSNPrs3087879
23andMers3087879
SNPshotrs3087879
SNPdbers3087879
MSV3drs3087879
GWAS Ctlgrs3087879
GMAF0.2374
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 19349310OA-icon.png] 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 19324536OA-icon.png] 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,