rs1553264218
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1558182956
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
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 |
rs201286421
|
|
T |
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 |
rs201286421
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.
|
21106325 |
2011 |
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 |
Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation.
|
22868853 |
2012 |
rs587776652
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
|
11062460 |
2000 |
rs587776652
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3.
|
22351710 |
2012 |
rs587776653
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC.
|
12658451 |
2003 |
rs587776653
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).
|
24758179 |
2014 |
rs587776653
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC.
|
12658451 |
2003 |
rs587776653
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
|
22517554 |
2012 |
rs587776653
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs587776653
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma.
|
15342702 |
2004 |
rs587776653
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
|
22517554 |
2012 |
rs587776653
|
|
T |
0.700 |
GeneticVariation |
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 |
rs587776653
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).
|
24758179 |
2014 |
rs587776653
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Functional cardiac paraganglioma associated with a rare SDHC mutation.
|
24402737 |
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 |
Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.
|
19351833 |
2009 |
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 |
rs587778661
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
|
27279923 |
2016 |
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 |
rs755235380
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3.
|
22351710 |
2012 |