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rs4759802

From SNPedia

Orientationplus
Stabilizedplus
Make rs4759802(A;A)
Make rs4759802(A;G)
Make rs4759802(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position130922632
is asnp
is mentioned by
dbSNPrs4759802
dbSNP (old)rs4759802
ClinGenrs4759802
ebirs4759802
HLIrs4759802
Exacrs4759802
Gnomadrs4759802
Varsomers4759802
Maprs4759802
PheGenIrs4759802
Biobankrs4759802
1000 genomesrs4759802
hgdprs4759802
ensemblrs4759802
gopubmedrs4759802
geneviewrs4759802
scholarrs4759802
googlers4759802
pharmgkbrs4759802
gwascentralrs4759802
openSNPrs4759802
23andMers4759802
23andMe allrs4759802
SNP Nexus

SNPshotrs4759802
SNPdbers4759802
MSV3drs4759802
GWAS Ctlgrs4759802
GMAF0.1795
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs4759802
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.820312
summary