Gene: SUFU ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554841447
rs1554841447
SUFU
A 0.700 GeneticVariation CLINVAR Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations. 25403219

2014
dbSNP: rs1564676479
rs1564676479
SUFU
A 0.700 GeneticVariation 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 Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations. 25403219

2014
dbSNP: rs1554841447
rs1554841447
SUFU
A 0.700 GeneticVariation CLINVAR High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age. 22508808

2012
dbSNP: rs1554852279
rs1554852279
SUFU
TTA 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: rs1564676479
rs1564676479
SUFU
A 0.700 GeneticVariation 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 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
dbSNP: rs1060501105
rs1060501105
SUFU
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501108
rs1060501108
SUFU
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501109
rs1060501109
SUFU
T 0.700 CausalMutation CLINVAR

dbSNP: rs1477199832
rs1477199832
SUFU
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1554840869
rs1554840869
ACTR1A ; SUFU
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1564654588
rs1564654588
ACTR1A ; SUFU
T 0.700 CausalMutation CLINVAR

dbSNP: rs1564698683
rs1564698683
SUFU
A 0.700 CausalMutation CLINVAR

dbSNP: rs1564698850
rs1564698850
SUFU
CTGTGT 0.700 CausalMutation CLINVAR

dbSNP: rs28942088
rs28942088
ACTR1A ; SUFU
T 0.700 CausalMutation CLINVAR

dbSNP: rs863224925
rs863224925
ACTR1A ; SUFU
T 0.700 CausalMutation CLINVAR