Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas. 21945342

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas. 21945342

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients? 21792967

2011
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Genetics of pheochromocytoma and paraganglioma in Spanish patients. 19258401

2009
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Novel SDHD germ-line mutations in pheochromocytoma patients. 17576205

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
A 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
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 A role for mitochondrial enzymes in inherited neoplasia and beyond. 12612654

2003
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinese family: a founder effect? 12782822

2003
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR A role for mitochondrial enzymes in inherited neoplasia and beyond. 12612654

2003
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. 11391796

2001