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rs4508864

From SNPedia

Orientationplus
Stabilizedplus
Make rs4508864(C;C)
Make rs4508864(C;T)
Make rs4508864(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154560137
is asnp
is mentioned by
dbSNPrs4508864
dbSNP (classic)rs4508864
ClinGenrs4508864
ebirs4508864
HLIrs4508864
Exacrs4508864
Gnomadrs4508864
Varsomers4508864
LitVarrs4508864
Maprs4508864
PheGenIrs4508864
Biobankrs4508864
1000 genomesrs4508864
hgdprs4508864
ensemblrs4508864
geneviewrs4508864
scholarrs4508864
googlers4508864
pharmgkbrs4508864
gwascentralrs4508864
openSNPrs4508864
23andMers4508864
SNPshotrs4508864
SNPdbers4508864
MSV3drs4508864
GWAS Ctlgrs4508864
GMAF0.1974
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23144326OA-icon.png]
Trait Chronic obstructive pulmonary disease-related biomarkers
Title Genome-Wide Association Analysis of Blood Biomarkers in Chronic Obstructive Pulmonary Disease.
Risk Allele T
P-val 6E-6
Odds Ratio NR NR


[PMID 20031576OA-icon.png] Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.