Disease: Neoplastic Syndromes, Hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755047928
rs755047928
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5. 26273102 2015
dbSNP: rs755047928
rs755047928
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad. 24859990 2014
dbSNP: rs755047928
rs755047928
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. 19576851 2009
dbSNP: rs755047928
rs755047928
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582 2009
dbSNP: rs755047928
rs755047928
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR High prevalence of SDHB mutations in head and neck paraganglioma in Belgium. 18551016 2008