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rs4705952

From SNPedia

Orientationplus
Stabilizedplus
Make rs4705952(A;A)
Make rs4705952(A;G)
Make rs4705952(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132503926
is asnp
is mentioned by
dbSNPrs4705952
dbSNP (classic)rs4705952
ClinGenrs4705952
ebirs4705952
HLIrs4705952
Exacrs4705952
Gnomadrs4705952
Varsomers4705952
LitVarrs4705952
Maprs4705952
PheGenIrs4705952
Biobankrs4705952
1000 genomesrs4705952
hgdprs4705952
ensemblrs4705952
geneviewrs4705952
scholarrs4705952
googlers4705952
pharmgkbrs4705952
gwascentralrs4705952
openSNPrs4705952
23andMers4705952
SNPshotrs4705952
SNPdbers4705952
MSV3drs4705952
GWAS Ctlgrs4705952
GMAF0.4421
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21300955OA-icon.png]
Trait
Title Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
Risk Allele G
P-val 1E-8
Odds Ratio 0.0420 [0.03-0.05] unit increase

[PMID 19145247OA-icon.png] Lack of association of interferon regulatory factor 1 with severe malaria in affected child-parental trio studies across three African populations.