Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
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 |
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|
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 |
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|
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 |
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|
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 |
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|
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 |
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|
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 |
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|
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 |
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|
A | 0.700 | CausalMutation | CLINVAR | Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma. | 21188540 | 2011 |
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|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
GC | 0.700 | CausalMutation | CLINVAR | ||||||
|
TC | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
CTGTGT | 0.700 | CausalMutation | CLINVAR |