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rs1379357

From SNPedia

Orientationminus
Stabilizedminus
Make rs1379357(C;C)
Make rs1379357(C;G)
Make rs1379357(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position24924066
is asnp
is mentioned by
dbSNPrs1379357
ebirs1379357
HLIrs1379357
Exacrs1379357
Varsomers1379357
Maprs1379357
PheGenIrs1379357
hapmaprs1379357
1000 genomesrs1379357
hgdprs1379357
ensemblrs1379357
gopubmedrs1379357
geneviewrs1379357
scholarrs1379357
googlers1379357
pharmgkbrs1379357
gwascentralrs1379357
openSNPrs1379357
23andMers1379357
23andMe allrs1379357
SNP Nexus

SNPshotrs1379357
SNPdbers1379357
MSV3drs1379357
GWAS Ctlgrs1379357
GMAF0.4761
Max Magnitude
GET Evidence
rs1379357
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.414062
summary