| Gene | Disease | Score gda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
0.400 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.460 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.310 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.320 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.310 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.350 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.470 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.600 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.600 | Biomarker | GENOMICS_ENGLAND | A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation. | 10545598 | 1999 |
||||||||
|
|
0.700 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.450 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.460 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.500 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.320 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.360 | Biomarker | GENOMICS_ENGLAND | Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges. | 24627108 | 2014 |
||||||||
|
|
0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.440 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.440 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.300 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.410 | Biomarker | GENOMICS_ENGLAND | |||||||||||
|
|
0.410 | Biomarker | GENOMICS_ENGLAND |