Gene: SDHD ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. 27279923

2016
dbSNP: rs80338843
rs80338843
SDHD ; TIMM8B
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
dbSNP: rs80338844
rs80338844
SDHD
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
dbSNP: rs80338845
rs80338845
SDHD
T 0.700 CausalMutation CLINVAR A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. 26008905

2015
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Challenges in the diagnosis of pheochromocytoma and paraganglioma syndrome. 25275255

2014
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498

2013
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444

2013
dbSNP: rs104894305
rs104894305
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498

2013
dbSNP: rs1131691065
rs1131691065
SDHD
A 0.700 CausalMutation CLINVAR Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. 23512077

2013
dbSNP: rs387906358
rs387906358
SDHD
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
dbSNP: rs80338844
rs80338844
SDHD
T 0.700 CausalMutation CLINVAR Genetic testing in head and neck paraganglioma: who, what, and why? 24436918

2013
dbSNP: rs80338844
rs80338844
SDHD
T 0.700 CausalMutation CLINVAR Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. 23433498

2013
dbSNP: rs104894302
rs104894302
SDHD
T 0.700 GeneticVariation CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717

2012
dbSNP: rs104894304
rs104894304
SDHD
G 0.700 CausalMutation CLINVAR The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression. 22456618

2012
dbSNP: rs104894306
rs104894306
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866

2012
dbSNP: rs104894306
rs104894306
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717

2012
dbSNP: rs104894306
rs104894306
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554

2012
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
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
dbSNP: rs104894307
rs104894307
SDHD ; TIMM8B
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
dbSNP: rs1050032491
rs1050032491
SDHD
A 0.700 CausalMutation CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
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
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
C 0.700 CausalMutation CLINVAR Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717

2012
dbSNP: rs80338842
rs80338842
SDHD ; TIMM8B
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
dbSNP: rs80338843
rs80338843
SDHD ; TIMM8B
T 0.700 CausalMutation CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866

2012