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rs301430

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs301430(C;C)
Make rs301430(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position4576680
GeneSLC1A1, SPATA6L
is asnp
is mentioned by
dbSNPrs301430
dbSNP (classic)rs301430
ClinGenrs301430
ebirs301430
HLIrs301430
Exacrs301430
Gnomadrs301430
Varsomers301430
LitVarrs301430
Maprs301430
PheGenIrs301430
Biobankrs301430
1000 genomesrs301430
hgdprs301430
ensemblrs301430
geneviewrs301430
scholarrs301430
googlers301430
pharmgkbrs301430
gwascentralrs301430
openSNPrs301430
23andMers301430
SNPshotrs301430
SNPdbers301430
MSV3drs301430
GWAS Ctlgrs301430
GMAF0.4486
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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


[PMID 20155310OA-icon.png] Brief Report: Glutamate Transporter Gene (SLC1A1) Single Nucleotide Polymorphism (rs301430) and Repetitive Behaviors and Anxiety in Children with Autism Spectrum Disorder

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


[PMID 23564280] Association between SLC1A1 gene and early-onset OCD in the Han Chinese population: a case-control study.


[PMID 23411042] Association of the candidate gene SLC1A1 and obsessive-compulsive disorder in Han Chinese population


ClinVar
Risk rs301430(C;C)
Alt rs301430(C;C)
Reference Rs301430(T;T)
Significance Non-pathogenic
Disease Dicarboxylic aminoaciduria
Variation info
Gene SPATA6L SLC1A1
CLNDBN Dicarboxylic aminoaciduria
Reversed 0
HGVS NC_000009.11:g.4576680T>C
CLNSRC
CLNACC RCV000402585.1,