Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
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0.800 | GeneticVariation | UNIPROT | Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. | 26522469 | 2015 | |||||||
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0.800 | GeneticVariation | UNIPROT | Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. | 26522469 | 2015 | |||||||
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0.800 | GeneticVariation | UNIPROT | Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. | 26522469 | 2015 | |||||||
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|
|
G | 0.800 | CausalMutation | CLINVAR | |||||||||
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T | 0.800 | CausalMutation | CLINVAR | |||||||||
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T | 0.800 | CausalMutation | CLINVAR | |||||||||
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0.700 | GeneticVariation | GWASCAT | Leveraging Polygenic Functional Enrichment to Improve GWAS Power. | 30595370 | 2019 | |||||||
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|
0.700 | GeneticVariation | GWASCAT | Leveraging Polygenic Functional Enrichment to Improve GWAS Power. | 30595370 | 2019 | |||||||
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0.700 | GeneticVariation | GWASCAT | Leveraging Polygenic Functional Enrichment to Improve GWAS Power. | 30595370 | 2019 | |||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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|
A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Discovery of common and rare genetic risk variants for colorectal cancer. | 30510241 | 2019 | ||||||
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|
|
0.700 | GeneticVariation | GWASCAT | Leveraging Polygenic Functional Enrichment to Improve GWAS Power. | 30595370 | 2019 | |||||||
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|
A | 0.700 | GeneticVariation | GWASCAT | Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. | 29391396 | 2018 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. | 29391396 | 2018 | ||||||
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0.700 | GeneticVariation | GWASCAT | Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. | 29124443 | 2018 | |||||||
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0.700 | GeneticVariation | GWASCAT | Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. | 29124443 | 2018 | |||||||
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0.700 | GeneticVariation | GWASCAT | Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. | 29124443 | 2018 |