Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444

2013

dbSNP: rs786203251
rs786203251
T 0.700 GeneticVariation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444

2013

dbSNP: rs786203251
rs786203251
T 0.700 GeneticVariation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554

2012

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554

2012

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function. 22835832

2012

dbSNP: rs786203251
rs786203251
T 0.700 GeneticVariation CLINVAR Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations. 21173220

2011

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management. 20208144

2010

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. 19802898

2010

dbSNP: rs786203251
rs786203251
T 0.700 GeneticVariation 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: rs786203251
rs786203251
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: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Paraganglioma syndrome: SDHB, SDHC, and SDHD mutations in head and neck paragangliomas. 17102086

2006

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Effects of compression on physiologic integrity of the spinal cord, on circulation, and clinical status in four different directions of compression: posterior, anterior, circumferential, and lateral. 1523504

1992