rs1800789

Orientation

plus

Stabilized

plus

Make rs1800789(A;A)

Make rs1800789(A;G)

Make rs1800789(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154561591

Gene

FGB

is a	snp
is	mentioned by
dbSNP	rs1800789
dbSNP (classic)	rs1800789
ClinGen	rs1800789
ebi	rs1800789
HLI	rs1800789
Exac	rs1800789
Gnomad	rs1800789
Varsome	rs1800789
LitVar	rs1800789
Map	rs1800789
PheGenI	rs1800789
Biobank	rs1800789
1000 genomes	rs1800789
hgdp	rs1800789
ensembl	rs1800789
geneview	rs1800789
scholar	rs1800789
google	rs1800789
pharmgkb	rs1800789
gwascentral	rs1800789
openSNP	rs1800789
23andMe	rs1800789
SNPshot	rs1800789
SNPdbe	rs1800789
MSV3d	rs1800789
GWAS Ctlg	rs1800789

GMAF

0.1763

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

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

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

GWAS snp
PMID	[PMID 23969696]
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

[PMID 32214403] Evaluation of single nucleotide polymorphisms in 6 candidate genes and carotid intima-media thickness in community-dwelling residents.