rs587776653, SDHC

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR Functional cardiac paraganglioma associated with a rare SDHC mutation. 24402737 2014
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR Functional cardiac paraganglioma associated with a rare SDHC mutation. 24402737 2014
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). 24758179 2014
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). 24758179 2014
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). 24758179 2014
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). 24758179 2014
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554 2012
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554 2012
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554 2012
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554 2012
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
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
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
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
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. 16249420 2005
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. 15342702 2004
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. 15342702 2004
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451 2003
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 GeneticVariation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451 2003
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451 2003
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451 2003
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 GeneticVariation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451 2003
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
0.700 CausalMutation CLINVAR
PARAGANGLIOMAS 3
CUI: C1854336
Disease: PARAGANGLIOMAS 3
0.700 CausalMutation CLINVAR
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR
Pulmonary chondroma
CUI: C3203483
Disease: Pulmonary chondroma
0.700 GeneticVariation CLINVAR
Carney Triad
CUI: C1858592
Disease: Carney Triad
0.700 GeneticVariation CLINVAR