rs80338844
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
rs80338844
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Canadian guideline on genetic screening for hereditary renal cell cancers.
|
24319509 |
2013 |
rs80338844
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
|
24893135 |
2014 |
rs80338845
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
|
24893135 |
2014 |
rs80338845
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Canadian guideline on genetic screening for hereditary renal cell cancers.
|
24319509 |
2013 |
rs80338845
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
rs104894302
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Novel SDHD gene mutation (H102R) in a patient with metastatic cervical paraganglioma effectively treated by peptide receptor radionuclide therapy.
|
22025150 |
2011 |
rs104894302
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
|
10657297 |
2000 |
rs104894302
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
|
22241717 |
2012 |
rs104894302
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.
|
12811540 |
2003 |
rs104894302
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
rs1060503773
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555187083
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.
|
16317055 |
2006 |
rs1566691921
|
|
TT |
0.700 |
GeneticVariation |
CLINVAR |
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.
|
19802898 |
2010 |
rs1566691921
|
|
TT |
0.700 |
GeneticVariation |
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
rs864321644
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs876658477
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas.
|
15479192 |
2004 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect.
|
21937622 |
2011 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
|
11897817 |
2002 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
|
10657297 |
2000 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Genetic testing in head and neck paraganglioma: who, what, and why?
|
24436918 |
2013 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
|
11391796 |
2001 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
|
23433498 |
2013 |
rs80338844
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
|
21348866 |
2012 |