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rs2179652

From SNPedia

Orientationplus
Stabilizedplus
Make rs2179652(C;C)
Make rs2179652(C;T)
Make rs2179652(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position192800696
GeneLOC100130137
is asnp
is mentioned by
dbSNPrs2179652
dbSNP (classic)rs2179652
ClinGenrs2179652
ebirs2179652
HLIrs2179652
Exacrs2179652
Gnomadrs2179652
Varsomers2179652
LitVarrs2179652
Maprs2179652
PheGenIrs2179652
Biobankrs2179652
1000 genomesrs2179652
hgdprs2179652
ensemblrs2179652
geneviewrs2179652
scholarrs2179652
googlers2179652
pharmgkbrs2179652
gwascentralrs2179652
openSNPrs2179652
23andMers2179652
SNPshotrs2179652
SNPdbers2179652
MSV3drs2179652
GWAS Ctlgrs2179652
GMAF0.4279
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 18347610] Further evidence for association of the RGS2 gene with antipsychotic-induced parkinsonism: protective role of a functional polymorphism in the 3'-untranslated region


[PMID 18262772OA-icon.png] Association of RGS2 and RGS5 variants with schizophrenia symptom severity.


[PMID 20386734OA-icon.png] Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis.