Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
G | 0.800 | GeneticVariation | CLINVAR | ||||||||||
|
|
C | 0.800 | CausalMutation | CLINVAR | ||||||||||
|
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory. | 16301862 | 2006 |
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|
|
C | 0.700 | CausalMutation | CLINVAR | PTCH mutations: distribution and analyses. | 16419085 | 2006 |
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|
|
C | 0.700 | GeneticVariation | CLINVAR | Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory. | 16301862 | 2006 |
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|
|
C | 0.700 | GeneticVariation | CLINVAR | PTCH mutations: distribution and analyses. | 16419085 | 2006 |
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|
|
G | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
A | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||||||
|
|
A | 0.700 | CausalMutation | CLINVAR | Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. | 8981943 | 1997 |
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|
|
A | 0.700 | CausalMutation | CLINVAR | Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory. | 16301862 | 2006 |
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|
|
CT | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
CT | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
A | 0.700 | CausalMutation | CLINVAR | Patched mutations and hairy skin patches: a new sign in Gorlin syndrome. | 16906569 | 2006 |
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|
|
T | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
G | 0.700 | CausalMutation | CLINVAR |