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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
dbSNP (classic)rs2301753
ClinGenrs2301753
ebirs2301753
HLIrs2301753
Exacrs2301753
Gnomadrs2301753
Varsomers2301753
LitVarrs2301753
Maprs2301753
PheGenIrs2301753
Biobankrs2301753
1000 genomesrs2301753
hgdprs2301753
ensemblrs2301753
geneviewrs2301753
scholarrs2301753
googlers2301753
pharmgkbrs2301753
gwascentralrs2301753
openSNPrs2301753
23andMers2301753
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.



[PMID 26534935OA-icon.png] Genetic Loci Associated With Nonobstructive Coronary Artery Disease in Caucasian Women