Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360 2017
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360 2017
dbSNP: rs74315370
rs74315370
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
C 0.800 CausalMutation CLINVAR Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma. 28738844 2017
dbSNP: rs74315372
rs74315372
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360 2017
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360 2017
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
T 0.800 GeneticVariation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882 2016
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
T 0.800 CausalMutation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882 2016
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
T 0.800 CausalMutation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882 2016
dbSNP: rs138996609
rs138996609
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
A 0.800 CausalMutation CLINVAR Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma. 25873086 2015
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
T 0.800 CausalMutation CLINVAR Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy. 25736212 2015
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
T 0.800 CausalMutation CLINVAR Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy. 25736212 2015
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
T 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
dbSNP: rs74315368
rs74315368
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
T 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
dbSNP: rs74315370
rs74315370
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
C 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
dbSNP: rs74315372
rs74315372
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
dbSNP: rs74315372
rs74315372
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
0.800 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
T 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0031511
Disease:
Pheochromocytoma
T 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015
dbSNP: rs772551056
rs772551056
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4
T 0.800 GeneticVariation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245 2015