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rs7313149

From SNPedia

Orientationplus
Stabilizedplus
Make rs7313149(C;C)
Make rs7313149(C;T)
Make rs7313149(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position13675353
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs7313149
ebirs7313149
HLIrs7313149
Exacrs7313149
Varsomers7313149
Maprs7313149
PheGenIrs7313149
hapmaprs7313149
1000 genomesrs7313149
hgdprs7313149
ensemblrs7313149
gopubmedrs7313149
geneviewrs7313149
scholarrs7313149
googlers7313149
pharmgkbrs7313149
gwascentralrs7313149
openSNPrs7313149
23andMers7313149
23andMe allrs7313149
SNP Nexus

SNPshotrs7313149
SNPdbers7313149
MSV3drs7313149
GWAS Ctlgrs7313149
GMAF0.2075
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7313149
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.234375
summary