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rs1800789

From SNPedia

Orientationplus
Stabilizedplus
Make rs1800789(A;A)
Make rs1800789(A;G)
Make rs1800789(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154561591
GeneFGB
is asnp
is mentioned by
dbSNPrs1800789
ebirs1800789
HLIrs1800789
Exacrs1800789
Varsomers1800789
Maprs1800789
PheGenIrs1800789
hapmaprs1800789
1000 genomesrs1800789
hgdprs1800789
ensemblrs1800789
gopubmedrs1800789
geneviewrs1800789
scholarrs1800789
googlers1800789
pharmgkbrs1800789
gwascentralrs1800789
openSNPrs1800789
23andMers1800789
23andMe allrs1800789
SNP Nexus

SNPshotrs1800789
SNPdbers1800789
MSV3drs1800789
GWAS Ctlgrs1800789
GMAF0.1763
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20031576OA-icon.png] Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts


[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study


GET Evidence
rs1800789
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary



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 2E-127
Odds Ratio .03 [0.029-0.033] unit increase