Disease: PARAGANGLIOMAS 4 ×
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: 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: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. 24893135 2014
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Canadian guideline on genetic screening for hereditary renal cell cancers. 24319509 2013
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility. 20065170 2010
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Endocrine cancer predisposition syndromes: hereditary paraganglioma, multiple endocrine neoplasia type 1, multiple endocrine neoplasia type 2, and hereditary thyroid cancer. 20816580 2010
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas. 14715873 2004
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326 2004
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility. 14974914 2003
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. 11897817 2002
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		0.800 GeneticVariation UNIPROT Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. 11404820 2001
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		C 0.800 GeneticVariation CLINVAR
dbSNP: rs74315367
rs74315367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C1861848
Disease:
PARAGANGLIOMAS 4 		C 0.800 CausalMutation CLINVAR