rs786201095
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
|
29386252 |
2018 |
rs202101384
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling.
|
27604842 |
2017 |
rs74315370
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma.
|
28738844 |
2017 |
rs751000085
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The phenotype of SDHB germline mutation carriers: a nationwide study.
|
28490599 |
2017 |
rs786201095
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
|
28349240 |
2017 |
rs786201095
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations.
|
28374168 |
2017 |
rs202101384
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy.
|
26642834 |
2016 |
rs397516833
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation.
|
27549546 |
2016 |
rs587782604
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
|
27539324 |
2016 |
rs587782604
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
|
27539324 |
2016 |
rs772551056
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery.
|
26719882 |
2016 |
rs786201063
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
|
27539324 |
2016 |
rs786201095
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Carney triad can be (rarely) associated with germline succinate dehydrogenase defects.
|
26173966 |
2016 |
rs138996609
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma.
|
25873086 |
2015 |
rs1557739966
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.
|
26273102 |
2015 |
rs202101384
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance.
|
26925370 |
2015 |
rs267607032
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Paraganglioma Presenting as Postpartum Fever of Unknown Origin.
|
26236513 |
2015 |
rs398123690
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population.
|
26267327 |
2015 |
rs587782604
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
SDHD immunohistochemistry: a new tool to validate SDHx mutations in pheochromocytoma/paraganglioma.
|
25405498 |
2015 |
rs587782604
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice.
|
25695889 |
2015 |
rs587782604
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
[Intrapericardical paraganglioma associated with mutation in succinate dehydrogenase enzyme gene].
|
24939699 |
2015 |
rs587782604
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.
|
26259135 |
2015 |
rs587782604
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.
|
26259135 |
2015 |
rs74315368
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy.
|
25736212 |
2015 |
rs74315368
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Structural and functional consequences of succinate dehydrogenase subunit B mutations.
|
25972245 |
2015 |