Disease: Familial primary pulmonary hypertension ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852741
rs137852741
Entrez Id: 659
Gene Symbol: BMPR2
BMPR2
CUI: C0340543
Disease:
Familial primary pulmonary hypertension 		0.010 GeneticVariation BEFREE Lipid content was assessed in rodent and human HPAH RVs and in Rosa26(R899X) mice after metformin administration. 24274756 2014
dbSNP: rs137852746
rs137852746
Entrez Id: 659
Gene Symbol: BMPR2
BMPR2
CUI: C0340543
Disease:
Familial primary pulmonary hypertension 		0.010 GeneticVariation BEFREE Bone morphogenetic protein receptor-II mutation Arg491Trp causes malignant phenotype of familial primary pulmonary hypertension. 14985116 2004