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rs2301753

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2301753(A;A)
Make rs2301753(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position30071463
GeneRNF39
is asnp
is mentioned by
dbSNPrs2301753
ebirs2301753
HLIrs2301753
Exacrs2301753
Varsomers2301753
Maprs2301753
PheGenIrs2301753
hapmaprs2301753
1000 genomesrs2301753
hgdprs2301753
ensemblrs2301753
gopubmedrs2301753
geneviewrs2301753
scholarrs2301753
googlers2301753
pharmgkbrs2301753
gwascentralrs2301753
openSNPrs2301753
23andMers2301753
23andMe allrs2301753
SNP Nexus

SNPshotrs2301753
SNPdbers2301753
MSV3drs2301753
GWAS Ctlgrs2301753
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 18982067OA-icon.png] HIV-1 disease-influencing effects associated with ZNRD1, HCP5 and HLA-C alleles are attributable mainly to either HLA-A10 or HLA-B*57 alleles.


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


GET Evidence
RNF39-A304E
aa_change Ala304Glu
aa_change_short A304E
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.173041
summary



[PMID 26534935] Genetic Loci Associated With Nonobstructive Coronary Artery Disease in Caucasian Women