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rs1154988

From SNPedia

Orientationplus
Stabilizedplus
Make rs1154988(A;A)
Make rs1154988(A;T)
Make rs1154988(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position136206349
is asnp
is mentioned by
dbSNPrs1154988
ebirs1154988
HLIrs1154988
Exacrs1154988
Varsomers1154988
Maprs1154988
PheGenIrs1154988
hapmaprs1154988
1000 genomesrs1154988
hgdprs1154988
ensemblrs1154988
gopubmedrs1154988
geneviewrs1154988
scholarrs1154988
googlers1154988
pharmgkbrs1154988
gwascentralrs1154988
openSNPrs1154988
23andMers1154988
23andMe allrs1154988
SNP Nexus

SNPshotrs1154988
SNPdbers1154988
MSV3drs1154988
GWAS Ctlgrs1154988
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23969696OA-icon.png]
Trait Fibrinogen
Title Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Risk Allele A
P-val 1E-16
Odds Ratio .01 [0.008-0.012] unit decrease