Have questions? Visit https://www.reddit.com/r/SNPedia

rs3794087

From SNPedia

Orientationminus
Stabilizedminus
Make rs3794087(A;A)
Make rs3794087(A;C)
Make rs3794087(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position35308068
GeneSLC1A2
is asnp
is mentioned by
dbSNPrs3794087
ebirs3794087
HLIrs3794087
Exacrs3794087
Varsomers3794087
Maprs3794087
PheGenIrs3794087
hapmaprs3794087
1000 genomesrs3794087
hgdprs3794087
ensemblrs3794087
gopubmedrs3794087
geneviewrs3794087
scholarrs3794087
googlers3794087
pharmgkbrs3794087
gwascentralrs3794087
openSNPrs3794087
23andMers3794087
23andMe allrs3794087
SNP Nexus

SNPshotrs3794087
SNPdbers3794087
MSV3drs3794087
GWAS Ctlgrs3794087
GMAF0.2158
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 22764253OA-icon.png] 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