| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.600 | Biomarker | disease | GENOMICS_ENGLAND | SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility. | 23539728 | 2013 | ||||
|
0.600 | GeneticVariation | disease | UNIPROT | SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility. | 23539728 | 2013 | ||||
|
0.600 | GeneticVariation | disease | UNIPROT | Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas. | 11297621 | 2001 | ||||
|
0.600 | Biomarker | disease | GENOMICS_ENGLAND | Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas. | 11297621 | 2001 | ||||
|
0.600 | CausalMutation | disease | CLINVAR | |||||||
|
0.600 | SusceptibilityMutation | disease | CLINVAR | |||||||
|
0.600 | CausalMutation | disease | CLINVAR | |||||||
|
0.400 | GeneticVariation | disease | UNIPROT | RAS point mutations and PAX8-PPAR gamma rearrangement in thyroid tumors: evidence for distinct molecular pathways in thyroid follicular carcinoma. | 12727991 | 2003 | ||||
|
0.400 | GeneticVariation | disease | UNIPROT | RAS point mutations and PAX8-PPAR gamma rearrangement in thyroid tumors: evidence for distinct molecular pathways in thyroid follicular carcinoma. | 12727991 | 2003 | ||||
|
0.400 | Biomarker | disease | GENOMICS_ENGLAND | Multiple hamartoma syndrome (Cowden's disease). | 4635800 | 1972 | ||||
|
0.400 | CausalMutation | disease | CLINVAR | |||||||
|
0.400 | CausalMutation | disease | CLINVAR | |||||||
|
0.400 | CausalMutation | disease | CLINVAR | |||||||
|
0.100 | CausalMutation | disease | CLINVAR |