rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
|
27279923 |
2016 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL.
|
27700540 |
2016 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Vascular Endothelial Growth Factor Receptor-Targeted Therapy in Succinate Dehydrogenase C Kidney Cancer.
|
25024072 |
2016 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations.
|
25394176 |
2015 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.
|
24781345 |
2014 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).
|
24758179 |
2014 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.
|
24728327 |
2014 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas.
|
24102379 |
2014 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
|
24523625 |
2014 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic variability and risk of malignancy in SDHC-linked paragangliomas: lessons from three unrelated cases with an identical germline mutation (p.Arg133*).
|
24423348 |
2014 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.
|
23666964 |
2013 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome.
|
23175444 |
2013 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
|
22703879 |
2012 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation.
|
22868853 |
2012 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer.
|
23083876 |
2012 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.
|
21106325 |
2011 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD.
|
17667967 |
2008 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma.
|
17898811 |
2007 |
rs1553261757
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553266474
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs587776653
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs898854295
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|