rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
|
29386252 |
2018 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Polymyalgia rheumatica and vagal paraganglioma.
|
28412079 |
2017 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Adrenocortical carcinoma and succinate dehydrogenase gene mutations: an observational case series.
|
28819017 |
2017 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
|
27279923 |
2016 |
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 |
AN AGGRESSIVE TEMPORAL BONE SDHC PARAGANGLIOMA ASSOCIATED WITH INCREASED HIF-2α SIGNALING.
|
26492543 |
2016 |
rs786205147
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Carney triad can be (rarely) associated with germline succinate dehydrogenase defects.
|
26173966 |
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 |
rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.
|
25494863 |
2015 |
rs786203457
|
|
G |
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 |
The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).
|
24758179 |
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 |
rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC-PGL syndromes: a clinicopathological and molecular analysis.
|
24096523 |
2014 |
rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Succinate dehydrogenase deficiency is rare in pituitary adenomas.
|
24625421 |
2014 |
rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients.
|
25025441 |
2014 |
rs786205147
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Succinate dehydrogenase deficient gastrointestinal stromal tumors (GISTs) - a review.
|
24886695 |
2014 |
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 |
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 |
rs755235380
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Immunohistochemical loss of succinate dehydrogenase subunit A (SDHA) in gastrointestinal stromal tumors (GISTs) signals SDHA germline mutation.
|
23282968 |
2013 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Immunohistochemical loss of succinate dehydrogenase subunit A (SDHA) in gastrointestinal stromal tumors (GISTs) signals SDHA germline mutation.
|
23282968 |
2013 |