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rs2596439

From SNPedia

Orientationplus
Stabilizedplus
Make rs2596439(A;A)
Make rs2596439(A;T)
Make rs2596439(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31372436
is asnp
is mentioned by
dbSNPrs2596439
ebirs2596439
HLIrs2596439
Exacrs2596439
Varsomers2596439
Maprs2596439
PheGenIrs2596439
hapmaprs2596439
1000 genomesrs2596439
hgdprs2596439
ensemblrs2596439
gopubmedrs2596439
geneviewrs2596439
scholarrs2596439
googlers2596439
pharmgkbrs2596439
gwascentralrs2596439
openSNPrs2596439
23andMers2596439
23andMe allrs2596439
SNP Nexus

SNPshotrs2596439
SNPdbers2596439
MSV3drs2596439
GWAS Ctlgrs2596439
GMAF0.4174
Max Magnitude


GET Evidence
rs2596439
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.554688
summary