Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
TGAAG | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | Analysis of all subunits, SDHA, SDHB, SDHC, SDHD, of the succinate dehydrogenase complex in KIT/PDGFRA wild-type GIST. | 23612575 | 2014 |
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|
T | 0.700 | CausalMutation | CLINVAR | Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention. | 28384794 | 2017 |
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|
T | 0.700 | CausalMutation | CLINVAR | SDHA is a tumor suppressor gene causing paraganglioma. | 20484225 | 2010 |
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|
T | 0.700 | CausalMutation | CLINVAR | Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients. | 26269449 | 2015 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | Associations of high-grade prostate cancer with BRCA1 and BRCA2 founder mutations. | 19188187 | 2009 |
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|
T | 0.700 | CausalMutation | CLINVAR | Cancer risks in BRCA2 families: estimates for sites other than breast and ovary. | 16141007 | 2005 |
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|
T | 0.700 | CausalMutation | CLINVAR | Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE. | 23628597 | 2013 |
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|
T | 0.700 | CausalMutation | CLINVAR | Risk of breast cancer in male BRCA2 carriers. | 20587410 | 2010 |
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|
T | 0.700 | CausalMutation | CLINVAR | Breast cancer risk among male BRCA1 and BRCA2 mutation carriers. | 18042939 | 2007 |
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|
T | 0.700 | CausalMutation | CLINVAR | Prevalence and characteristics of pancreatic cancer in families with BRCA1 and BRCA2 mutations. | 18855126 | 2009 |
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|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
G | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes. | 20142534 | 2010 |
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|
A | 0.700 | CausalMutation | CLINVAR | Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model. | 20883824 | 2011 |