Disease: Hamartoma Syndrome, Multiple ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199476086
rs199476086
Entrez Id: 657
Gene Symbol: BMPR1A
BMPR1A
CUI: C0018553
Disease:
Hamartoma Syndrome, Multiple 		0.010 GeneticVariation BEFREE One proband with CS/CS-like phenotype was also found to have a germline BMPR1A missense mutation (A338D). 11536076 2001