Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307307
rs1085307307
BMPR2
0.010 GeneticVariation BEFREE The predicted functional impact of the Glu386Val mutation and its absence in healthy controls support the mutation as the cause of FPAH. 18364108

2008