FBN2, fibrillin 2, 2201

N. diseases: 211; N. variants: 42
Disease: Systolic Pressure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17677603
rs17677603
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6595838
rs6595838
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs7705439
rs7705439
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs6595838
rs6595838
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. 28135244 2017
dbSNP: rs6595838
rs6595838
Entrez Id: 2201
Gene Symbol: FBN2
FBN2
CUI: C0871470
Disease:
Systolic Pressure 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017