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rs1044291

From SNPedia

Orientationplus
Stabilizedplus
Make rs1044291(C;C)
Make rs1044291(C;T)
Make rs1044291(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154572200
GeneFGB
is asnp
is mentioned by
dbSNPrs1044291
ebirs1044291
HLIrs1044291
Exacrs1044291
Varsomers1044291
Maprs1044291
PheGenIrs1044291
hapmaprs1044291
1000 genomesrs1044291
hgdprs1044291
ensemblrs1044291
gopubmedrs1044291
geneviewrs1044291
scholarrs1044291
googlers1044291
pharmgkbrs1044291
gwascentralrs1044291
openSNPrs1044291
23andMers1044291
23andMe allrs1044291
SNP Nexus

SNPshotrs1044291
SNPdbers1044291
MSV3drs1044291
GWAS Ctlgrs1044291
GMAF0.1993
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20135074] A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men


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


[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.