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

rs2301364

From SNPedia

Orientationplus
Stabilizedplus
Make rs2301364(C;C)
Make rs2301364(C;T)
Make rs2301364(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position137140083
GeneGRIN1
is asnp
is mentioned by
dbSNPrs2301364
dbSNP (classic)rs2301364
ClinGenrs2301364
ebirs2301364
HLIrs2301364
Exacrs2301364
Gnomadrs2301364
Varsomers2301364
LitVarrs2301364
Maprs2301364
PheGenIrs2301364
Biobankrs2301364
1000 genomesrs2301364
hgdprs2301364
ensemblrs2301364
geneviewrs2301364
scholarrs2301364
googlers2301364
pharmgkbrs2301364
gwascentralrs2301364
openSNPrs2301364
23andMers2301364
SNPshotrs2301364
SNPdbers2301364
MSV3drs2301364
GWAS Ctlgrs2301364
GMAF0.1703
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20438806] Association analysis of GRIN1 and GRIN2B polymorphisms and Parkinson's disease in a hospital-based case-control study