Gene: SDHD ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338844
rs80338844
SDHD
T 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009
dbSNP: rs104894308
rs104894308
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR W43X SDHD mutation in sporadic head and neck paraganglioma. 18561749

2008
dbSNP: rs104894308
rs104894308
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Paraganglioma after maternal transmission of a succinate dehydrogenase gene mutation. 18211978

2008
dbSNP: rs104894309
rs104894309
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1. 18826997

2008
dbSNP: rs1050032491
rs1050032491
SDHD
A 0.700 CausalMutation CLINVAR Mutations associated with succinate dehydrogenase D-related malignant paragangliomas. 17973943

2008
dbSNP: rs1306475361
rs1306475361
SDHD
T 0.700 CausalMutation CLINVAR High prevalence of SDHB mutations in head and neck paraganglioma in Belgium. 18551016

2008
dbSNP: rs587776649
rs587776649
SDHD ; TIMM8B
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
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Systematic screening and treatment evaluation of hereditary neck paragangliomas. 17563904

2007
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Novel SDHD germ-line mutations in pheochromocytoma patients. 17576205

2007
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR A Chinese family with familial paraganglioma syndrome due to succinate dehydrogenase deficiency. 17406045

2007
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Novel SDHD germ-line mutations in pheochromocytoma patients. 17576205

2007
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Novel SDHD germ-line mutations in pheochromocytoma patients. 17576205

2007
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055

2006
dbSNP: rs104894306
rs104894306
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055

2006
dbSNP: rs1555187083
rs1555187083
SDHD
A 0.700 GeneticVariation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055

2006
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Carotid body paraganglioma and SDHD mutation in a Greek family. 16080474

2005
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. 15066320

2004
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
G 0.700 CausalMutation CLINVAR Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. 15066320

2004
dbSNP: rs387906358
rs387906358
SDHD
A 0.700 CausalMutation CLINVAR The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features. 15235042

2004
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. 15066320

2004
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. 15066320

2004
dbSNP: rs80338843
rs80338843
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326

2004
dbSNP: rs80338844
rs80338844
SDHD
T 0.700 CausalMutation CLINVAR SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas. 15479192

2004
dbSNP: rs104894302
rs104894302
SDHD
T 0.700 GeneticVariation CLINVAR Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect. 12811540

2003
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
G 0.700 CausalMutation CLINVAR A role for mitochondrial enzymes in inherited neoplasia and beyond. 12612654

2003