rs1800792

Orientation

minus

Stabilized

minus

Make rs1800792(A;A)

Make rs1800792(A;G)

Make rs1800792(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

154613256

Gene

FGG

is a	snp
is	mentioned by
dbSNP	rs1800792
dbSNP (classic)	rs1800792
ClinGen	rs1800792
ebi	rs1800792
HLI	rs1800792
Exac	rs1800792
Gnomad	rs1800792
Varsome	rs1800792
LitVar	rs1800792
Map	rs1800792
PheGenI	rs1800792
Biobank	rs1800792
1000 genomes	rs1800792
hgdp	rs1800792
ensembl	rs1800792
geneview	rs1800792
scholar	rs1800792
google	rs1800792
pharmgkb	rs1800792
gwascentral	rs1800792
openSNP	rs1800792
23andMe	rs1800792
SNPshot	rs1800792
SNPdbe	rs1800792
MSV3d	rs1800792
GWAS Ctlg	rs1800792

GMAF

0.3062

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

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

[PMID 21137202] [Polymorphism of cytokine genes and human longevity]

[PMID 17827388 ] Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma.

[PMID 18974842 ] Gender differences in genetic risk profiles for cardiovascular disease.

[PMID 22273812 ] Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination Survey.