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rs1800788

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800788(C;C)
Make rs1800788(C;T)
Make rs1800788(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154562762
GeneFGB
is asnp
is mentioned by
dbSNPrs1800788
ebirs1800788
HLIrs1800788
Exacrs1800788
Varsomers1800788
Maprs1800788
PheGenIrs1800788
hapmaprs1800788
1000 genomesrs1800788
hgdprs1800788
ensemblrs1800788
gopubmedrs1800788
geneviewrs1800788
scholarrs1800788
googlers1800788
pharmgkbrs1800788
gwascentralrs1800788
openSNPrs1800788
23andMers1800788
23andMe allrs1800788
SNP Nexus

SNPshotrs1800788
SNPdbers1800788
MSV3drs1800788
GWAS Ctlgrs1800788
GMAF0.2732
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study
GWAS snp
PMID [PMID 21757653OA-icon.png]
Trait
Title Association of {gamma}' Fibrinogen With Cardiovascular Disease.
Risk Allele T
P-val 1E-39
Odds Ratio 0.1900 [0.16-0.22] g/L decrease


[PMID 22642105] [Polymorphic variants of genes encoding interleukin-6 and fibrinogen, the risk of ischemic stroke and fibrinogen levels]


[PMID 19272152OA-icon.png] IL6 and CRP haplotypes are associated with COPD risk and systemic inflammation: a case-control study.


[PMID 20031577OA-icon.png] Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.