| Gene | Disease | Score gda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
0.700 | CausalMutation | CLINVAR | |||||||||||
|
|
0.700 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.630 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.630 | CausalMutation | CLINVAR | |||||||||||
|
|
0.620 | CausalMutation | CLINVAR | |||||||||||
|
|
0.620 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.600 | CausalMutation | CLINVAR | |||||||||||
|
|
0.500 | CausalMutation | CLINVAR | Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families. | 22668073 | 2012 |
||||||||
|
|
0.500 | CausalMutation | CLINVAR | GJB2 mutations and degree of hearing loss: a multicenter study. | 16380907 | 2005 |
||||||||
|
|
0.500 | CausalMutation | CLINVAR | |||||||||||
|
|
0.500 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.500 | CausalMutation | CLINVAR | |||||||||||
|
|
0.500 | CausalMutation | CLINVAR | |||||||||||
|
|
0.500 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.480 | CausalMutation | CLINVAR | |||||||||||
|
|
0.480 | CausalMutation | CLINVAR | |||||||||||
|
|
0.480 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.470 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.470 | CausalMutation | CLINVAR | |||||||||||
|
|
0.460 | CausalMutation | CLINVAR | |||||||||||
|
|
0.450 | CausalMutation | CLINVAR | |||||||||||
|
|
0.430 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.430 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.430 | GeneticVariation | CLINVAR | |||||||||||
|
|
0.430 | CausalMutation | CLINVAR |