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

rs12920919

From SNPedia

Orientationplus
Stabilizedplus
Make rs12920919(C;C)
Make rs12920919(C;T)
Make rs12920919(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position9844123
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs12920919
ebirs12920919
HLIrs12920919
Exacrs12920919
Varsomers12920919
Maprs12920919
PheGenIrs12920919
hapmaprs12920919
1000 genomesrs12920919
hgdprs12920919
ensemblrs12920919
gopubmedrs12920919
geneviewrs12920919
scholarrs12920919
googlers12920919
pharmgkbrs12920919
gwascentralrs12920919
openSNPrs12920919
23andMers12920919
23andMe allrs12920919
SNP Nexus

SNPshotrs12920919
SNPdbers12920919
MSV3drs12920919
GWAS Ctlgrs12920919
GMAF0.2672
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs12920919
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.265625
summary