rs3794087
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3794087(A;A) |
Make rs3794087(A;C) |
Make rs3794087(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 35308068 |
Gene | SLC1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs3794087 |
dbSNP (classic) | rs3794087 |
ClinGen | rs3794087 |
ebi | rs3794087 |
HLI | rs3794087 |
Exac | rs3794087 |
Gnomad | rs3794087 |
Varsome | rs3794087 |
LitVar | rs3794087 |
Map | rs3794087 |
PheGenI | rs3794087 |
Biobank | rs3794087 |
1000 genomes | rs3794087 |
hgdp | rs3794087 |
ensembl | rs3794087 |
geneview | rs3794087 |
scholar | rs3794087 |
rs3794087 | |
pharmgkb | rs3794087 |
gwascentral | rs3794087 |
openSNP | rs3794087 |
23andMe | rs3794087 |
SNPshot | rs3794087 |
SNPdbe | rs3794087 |
MSV3d | rs3794087 |
GWAS Ctlg | rs3794087 |
GMAF | 0.2158 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22764253] Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor
[PMID 24424098] The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome
[PMID 23596072] SLC1A2 variant associated with essential tremor but not Parkinson disease in Chinese subjects.
[PMID 26313486] SLC1A2 rs3794087 variant and risk for essential tremor: a systematic review and meta-analysis
[PMID 31755235] Assessment of three essential tremor genetic loci in sporadic Parkinson's disease in Eastern China.