Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
0.450 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.400 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.400 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.400 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.300 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.300 | Biomarker | phenotype | GENOMICS_ENGLAND | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.100 | CausalMutation | phenotype | CLINVAR | |||||||
|
0.300 | Biomarker | phenotype | GENOMICS_ENGLAND | PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes. | 30858161 | 2019 |