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rs4751185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4751185(C;T)
Make rs4751185(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position130258151
is asnp
is mentioned by
dbSNPrs4751185
ebirs4751185
HLIrs4751185
Exacrs4751185
Varsomers4751185
Maprs4751185
PheGenIrs4751185
hapmaprs4751185
1000 genomesrs4751185
hgdprs4751185
ensemblrs4751185
gopubmedrs4751185
geneviewrs4751185
scholarrs4751185
googlers4751185
pharmgkbrs4751185
gwascentralrs4751185
openSNPrs4751185
23andMers4751185
23andMe allrs4751185
SNP Nexus

SNPshotrs4751185
SNPdbers4751185
MSV3drs4751185
GWAS Ctlgrs4751185
GMAF0.1065
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21160409OA-icon.png]
Trait
Title Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population
Risk Allele
P-val 0.000007
Odds Ratio None None