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rs2074480

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs2074480(A;C)
Make rs2074480(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position30073033
GeneRNF39
is asnp
is mentioned by
dbSNPrs2074480
ebirs2074480
HLIrs2074480
Exacrs2074480
Varsomers2074480
Maprs2074480
PheGenIrs2074480
hapmaprs2074480
1000 genomesrs2074480
hgdprs2074480
ensemblrs2074480
gopubmedrs2074480
geneviewrs2074480
scholarrs2074480
googlers2074480
pharmgkbrs2074480
gwascentralrs2074480
openSNPrs2074480
23andMers2074480
23andMe allrs2074480
SNP Nexus

SNPshotrs2074480
SNPdbers2074480
MSV3drs2074480
GWAS Ctlgrs2074480
GMAF0.1846
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 18495769OA-icon.png] Transmission of human immunodeficiency virus type 1 from a patient who developed AIDS to an elite suppressor.


[PMID 20041166OA-icon.png] Common genetic variation and the control of HIV-1 in humans.


GET Evidence
rs2074480
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.195312
summary