FBLN2, fibulin 2, 2199

N. diseases: 39; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061376
rs1061376
Entrez Id: 2199
Gene Symbol: FBLN2
FBLN2
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE For rs1061376, TT subjects had an OR for hypertension of 0.53 (95%CI: 0.32 to 0.87) compared with CC subjects, with reduced SBP (-7.91 mmHg; P = 0.008) and diastolic BP (DBP) (-3.69 mmHg; P = 0.015). 22912785 2012
dbSNP: rs3732666
rs3732666
Entrez Id: 2199
Gene Symbol: FBLN2
FBLN2
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE For rs3732666, the OR for hypertension in AG+GG subjects, compared with AA, was 0.71 (95%CI: 0.52 to 0.95). 22912785 2012