rs1057517818
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553265817
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs587776653
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs786202200
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs786205146
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs867966048
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs876658301
|
|
GT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs981049067
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
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 |
rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.
|
23666964 |
2013 |
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 |
Adrenocortical carcinoma and succinate dehydrogenase gene mutations: an observational case series.
|
28819017 |
2017 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
AN AGGRESSIVE TEMPORAL BONE SDHC PARAGANGLIOMA ASSOCIATED WITH INCREASED HIF-2α SIGNALING.
|
26492543 |
2016 |
rs587776653
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC.
|
12658451 |
2003 |
rs786205147
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Carney triad can be (rarely) associated with germline succinate dehydrogenase defects.
|
26173966 |
2016 |
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 |
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 |
rs755235380
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
rs786205147
|
|
A |
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 |
rs898854295
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Crystal structure of mitochondrial respiratory membrane protein complex II.
|
15989954 |
2005 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.
|
24781345 |
2014 |
rs764575966
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma.
|
17898811 |
2007 |
rs786203457
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma.
|
24150194 |
2013 |
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 |
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 |