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rs1800792

From SNPedia

Orientationminus
Stabilizedminus
Make rs1800792(A;A)
Make rs1800792(A;G)
Make rs1800792(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154613256
GeneFGG
is asnp
is mentioned by
dbSNPrs1800792
ebirs1800792
HLIrs1800792
Exacrs1800792
Varsomers1800792
Maprs1800792
PheGenIrs1800792
hapmaprs1800792
1000 genomesrs1800792
hgdprs1800792
ensemblrs1800792
gopubmedrs1800792
geneviewrs1800792
scholarrs1800792
googlers1800792
pharmgkbrs1800792
gwascentralrs1800792
openSNPrs1800792
23andMers1800792
23andMe allrs1800792
SNP Nexus

SNPshotrs1800792
SNPdbers1800792
MSV3drs1800792
GWAS Ctlgrs1800792
GMAF0.3062
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20167083OA-icon.png] 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 17827388OA-icon.png] Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma.


[PMID 18974842OA-icon.png] Gender differences in genetic risk profiles for cardiovascular disease.


[PMID 22273812OA-icon.png] 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.