rs104894304
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
|
27279923 |
2016 |
rs80338843
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
|
26269449 |
2015 |
rs80338844
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.
|
25494863 |
2015 |
rs80338845
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency.
|
26008905 |
2015 |
rs104894304
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome.
|
25275255 |
2014 |
rs104894304
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome.
|
23175444 |
2013 |
rs104894304
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
|
23433498 |
2013 |
rs104894305
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
|
23433498 |
2013 |
rs1131691065
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.
|
23512077 |
2013 |
rs387906358
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Identification of somatic VHL gene mutations in sporadic head and neck paragangliomas in association with activation of the HIF-1α/miR-210 signaling pathway.
|
23902947 |
2013 |
rs80338844
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic testing in head and neck paraganglioma: who, what, and why?
|
24436918 |
2013 |
rs80338844
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
|
23433498 |
2013 |
rs104894302
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
|
22241717 |
2012 |
rs104894304
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
|
22456618 |
2012 |
rs104894306
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
|
21348866 |
2012 |
rs104894306
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
|
22241717 |
2012 |
rs104894306
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
|
22517554 |
2012 |
rs104894307
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.
|
21945342 |
2012 |
rs104894307
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.
|
21945342 |
2012 |
rs1050032491
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
|
21348866 |
2012 |
rs80338842
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
|
22241717 |
2012 |
rs80338842
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
|
22241717 |
2012 |
rs80338842
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.
|
21945342 |
2012 |
rs80338842
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas.
|
21945342 |
2012 |
rs80338843
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.
|
21348866 |
2012 |