rs2074479
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs2074479(C;C) |
Make rs2074479(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 30073232 |
Gene | RNF39 |
is a | snp |
is | mentioned by |
dbSNP | rs2074479 |
dbSNP (classic) | rs2074479 |
ClinGen | rs2074479 |
ebi | rs2074479 |
HLI | rs2074479 |
Exac | rs2074479 |
Gnomad | rs2074479 |
Varsome | rs2074479 |
LitVar | rs2074479 |
Map | rs2074479 |
PheGenI | rs2074479 |
Biobank | rs2074479 |
1000 genomes | rs2074479 |
hgdp | rs2074479 |
ensembl | rs2074479 |
geneview | rs2074479 |
scholar | rs2074479 |
rs2074479 | |
pharmgkb | rs2074479 |
gwascentral | rs2074479 |
openSNP | rs2074479 |
23andMe | rs2074479 |
SNPshot | rs2074479 |
SNPdbe | rs2074479 |
MSV3d | rs2074479 |
GWAS Ctlg | rs2074479 |
GMAF | 0.1846 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18495769] Transmission of human immunodeficiency virus type 1 from a patient who developed AIDS to an elite suppressor.
[PMID 20041166] Common genetic variation and the control of HIV-1 in humans.