rs1554841447
|
|
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 |
rs1564676479
|
|
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 |
rs587776578
|
|
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 |
rs1554841447
|
|
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 |
rs1554852279
|
|
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 |
rs1564676479
|
|
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 |
rs587776578
|
|
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 |
rs587776578
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.
|
21188540 |
2011 |
rs1060501105
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1060501108
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060501109
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1477199832
|
|
GC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554840869
|
|
TC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1564654588
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1564698683
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1564698850
|
|
CTGTGT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs28942088
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs863224925
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|