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rs2074479

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2074479(C;C)
Make rs2074479(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position30073232
GeneRNF39
is asnp
is mentioned by
dbSNPrs2074479
ebirs2074479
HLIrs2074479
Exacrs2074479
Varsomers2074479
Maprs2074479
PheGenIrs2074479
hapmaprs2074479
1000 genomesrs2074479
hgdprs2074479
ensemblrs2074479
gopubmedrs2074479
geneviewrs2074479
scholarrs2074479
googlers2074479
pharmgkbrs2074479
gwascentralrs2074479
openSNPrs2074479
23andMers2074479
23andMe allrs2074479
SNP Nexus

SNPshotrs2074479
SNPdbers2074479
MSV3drs2074479
GWAS Ctlgrs2074479
GMAF0.1846
Max Magnitude0
? (C;C) (C;T) (T;T) 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
RNF39-S203P
aa_change Ser203Pro
aa_change_short S203P
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.176369
summary