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rs3780412

From SNPedia

Orientationminus
Stabilizedminus
Make rs3780412(A;A)
Make rs3780412(A;G)
Make rs3780412(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position4572480
GeneSLC1A1, SPATA6L
is asnp
is mentioned by
dbSNPrs3780412
ebirs3780412
HLIrs3780412
Exacrs3780412
Varsomers3780412
Maprs3780412
PheGenIrs3780412
hapmaprs3780412
1000 genomesrs3780412
hgdprs3780412
ensemblrs3780412
gopubmedrs3780412
geneviewrs3780412
scholarrs3780412
googlers3780412
pharmgkbrs3780412
gwascentralrs3780412
openSNPrs3780412
23andMers3780412
23andMe allrs3780412
SNP Nexus

SNPshotrs3780412
SNPdbers3780412
MSV3drs3780412
GWAS Ctlgrs3780412
GMAF0.4137
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19884611] Association of the glutamate transporter gene SLC1A1 with atypical antipsychotics-induced obsessive-compulsive symptoms


[PMID 16818867] Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.

[PMID 17894418] Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.

[PMID 19349310OA-icon.png] A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder.

[PMID 19360657OA-icon.png] Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample.

[PMID 22531293] Polymorphisms in the glutamate transporter gene SLC1A1 and obsessive-compulsive symptoms induced by second-generation antipsychotic agents.


GET Evidence
rs3780412
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.523438
summary