CACNA2D3, calcium voltage-gated channel auxiliary subunit alpha2delta 3, 55799
N. diseases: 33; N. variants: 14
Source: ALL
| Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
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0.700 | GeneticVariation | GWASCAT | Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy. | 31095341 | 2020 | |||||||
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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 | Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. | 29942086 | 2018 | ||||||
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C | 0.700 | GeneticVariation | GWASCAT | Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. | 30038396 | 2018 | ||||||
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G | 0.700 | GeneticVariation | GWASCAT | Co-regulatory networks of human serum proteins link genetics to disease. | 30072576 | 2018 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. | 29942086 | 2018 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. | 30038396 | 2018 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. | 27903959 | 2017 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence. | 28440896 | 2017 | ||||||
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G | 0.700 | GeneticVariation | GWASCAT | Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. | 27903959 | 2017 | ||||||
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A | 0.700 | GeneticVariation | GWASCAT | Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. | 27903959 | 2017 | ||||||
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0.020 | GeneticVariation | BEFREE | In conclusion, the combination of high red meat consumption, low menstrual blood loss and the HFE C282Y mutation may protect from iron deficiency in women of childbearing age. | 24663082 | 2014 | |||||||
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0.020 | GeneticVariation | BEFREE | This SNP along with the C282Y mutation explained significant differences in the distribution of individuals in three iron-related clinical phenotypes (normal, iron deficient and iron deficiency anaemic). | 23324578 | 2013 | |||||||
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0.010 | GeneticVariation | BEFREE | Novel SNP rs1375515, located in a subunit of the calcium channel gene CACNA2D3, is associated with a higher risk of anaemia. | 26460247 | 2015 | |||||||
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0.010 | GeneticVariation | BEFREE | The risk of developing anaemia is increased in reproductive age women carriers of A allele of rs1868505 (CACNA2D3) and/or T allele of rs13194491 (HIST1H2BJ). | 26460247 | 2015 |