FBN1, fibrillin 1, 2200

N. diseases: 552; N. variants: 1105
Disease: Hypertensive disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs668842
rs668842
Entrez Id: 2200
Gene Symbol: FBN1
FBN1
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE Haplotype G-T constructed of rs668842 and rs11635140 was significantly associated with hypertension comparing to reference haplotype A-C (P = 0.022). 24413999 2014