Disease: PARAGANGLIOMAS 2 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		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: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		0.800 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965 2015
dbSNP: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		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: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		0.800 GeneticVariation UNIPROT Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. 24893135 2014
dbSNP: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		0.800 GeneticVariation UNIPROT Canadian guideline on genetic screening for hereditary renal cell cancers. 24319509 2013
dbSNP: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		0.800 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
dbSNP: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		0.800 GeneticVariation UNIPROT American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility. 20065170 2010
dbSNP: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		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: rs113560320
rs113560320
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2
CUI: C1866552
Disease:
PARAGANGLIOMAS 2 (disorder) 		A 0.800 CausalMutation CLINVAR