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rs2070022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2070022(C;T)
Make rs2070022(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154583796
GeneFGA
is asnp
is mentioned by
dbSNPrs2070022
ebirs2070022
HLIrs2070022
Exacrs2070022
Varsomers2070022
Maprs2070022
PheGenIrs2070022
hapmaprs2070022
1000 genomesrs2070022
hgdprs2070022
ensemblrs2070022
gopubmedrs2070022
geneviewrs2070022
scholarrs2070022
googlers2070022
pharmgkbrs2070022
gwascentralrs2070022
openSNPrs2070022
23andMers2070022
23andMe allrs2070022
SNP Nexus

SNPshotrs2070022
SNPdbers2070022
MSV3drs2070022
GWAS Ctlgrs2070022
GMAF0.1612
Max Magnitude0
? (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 20416077OA-icon.png] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.

[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.