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rs2070016

From SNPedia

Orientationminus
Stabilizedminus
Make rs2070016(C;C)
Make rs2070016(C;T)
Make rs2070016(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589162
GeneFGA
is asnp
is mentioned by
dbSNPrs2070016
ebirs2070016
HLIrs2070016
Exacrs2070016
Varsomers2070016
Maprs2070016
PheGenIrs2070016
hapmaprs2070016
1000 genomesrs2070016
hgdprs2070016
ensemblrs2070016
gopubmedrs2070016
geneviewrs2070016
scholarrs2070016
googlers2070016
pharmgkbrs2070016
gwascentralrs2070016
openSNPrs2070016
23andMers2070016
23andMe allrs2070016
SNP Nexus

SNPshotrs2070016
SNPdbers2070016
MSV3drs2070016
GWAS Ctlgrs2070016
GMAF0.1341
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20167083OA-icon.png] Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study


[PMID 19190816] Association study between variants in the fibrinogen gene cluster, fibrinogen levels and hypertension: results from the MONICA/KORA study.


[PMID 19552680OA-icon.png] Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.


[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.