Variant: rs201286421 

    present in Gene: SDHC
    present in Chromosome: 1
    Position on Chromosome: 161323636
    Alleles of this Variant: C/T

rs201286421 in SDHC gene and Gastrointestinal Stromal Tumors PMID 24781345 2014 Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.

PMID 17667967 2008 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.

PMID 21106325 2011 Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.

PMID 19351833 2009 Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.

PMID 22868853 2012 Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation.

rs201286421 in SDHC gene and Hereditary Paraganglioma-Pheochromocytoma Syndrome PMID 17667967 2008 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.

PMID 22703879 2012 Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.

PMID 21106325 2011 Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.

PMID 24781345 2014 Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.

PMID 24758179 2014 The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).

PMID 22868853 2012 Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation.

rs201286421 in SDHC gene and Neoplastic Syndromes, Hereditary PMID 24758179 2014 The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).

PMID 22703879 2012 Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.

PMID 22868853 2012 Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation.

PMID 21106325 2011 Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.

PMID 19454582 2009 The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

PMID 24781345 2014 Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.

PMID 28412079 2017 Polymyalgia rheumatica and vagal paraganglioma.

PMID 27279923 2016 Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.

PMID 17667967 2008 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.

rs201286421 in SDHC gene and PARAGANGLIOMAS 3 PMID 22868853 2012 Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation.

PMID 24781345 2014 Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.

PMID 19351833 2009 Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out.

PMID 21106325 2011 Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.

PMID 17667967 2008 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.