Disease: Pheochromocytoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. 27279923 2016
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome. 25275255 2014
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444 2013
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498 2013
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression. 22456618 2012
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Systematic screening and treatment evaluation of hereditary neck paragangliomas. 17563904 2007
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055 2006
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Carotid body paraganglioma and SDHD mutation in a Greek family. 16080474 2005
dbSNP: rs104894304
rs104894304
Entrez Id: 6392
Gene Symbol: SDHD
SDHD
CUI: C0031511
Disease:
Pheochromocytoma 		G 0.700 CausalMutation CLINVAR Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma. 11343322 2001