Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776578
rs587776578
SUFU
A 0.700 CausalMutation CLINVAR Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations. 25403219

2014
dbSNP: rs587776578
rs587776578
SUFU
A 0.700 CausalMutation CLINVAR High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age. 22508808

2012
dbSNP: rs587776578
rs587776578
SUFU
A 0.700 CausalMutation CLINVAR Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma. 21188540

2011