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rs7674482

From SNPedia

Orientationplus
Stabilizedplus
Make rs7674482(C;C)
Make rs7674482(C;T)
Make rs7674482(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position45865444
is asnp
is mentioned by
dbSNPrs7674482
ebirs7674482
HLIrs7674482
Exacrs7674482
Varsomers7674482
Maprs7674482
PheGenIrs7674482
hapmaprs7674482
1000 genomesrs7674482
hgdprs7674482
ensemblrs7674482
gopubmedrs7674482
geneviewrs7674482
scholarrs7674482
googlers7674482
pharmgkbrs7674482
gwascentralrs7674482
openSNPrs7674482
23andMers7674482
23andMe allrs7674482
SNP Nexus

SNPshotrs7674482
SNPdbers7674482
MSV3drs7674482
GWAS Ctlgrs7674482
GMAF0.2801
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22174851OA-icon.png]
Trait
Title Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
Risk Allele
P-val 0.000005
Odds Ratio None None