Gene: SDHC ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755235380
rs755235380
SDHC
G 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009
dbSNP: rs786202200
rs786202200
SDHC
T 0.700 GeneticVariation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009
dbSNP: rs201286421
rs201286421
SDHC
T 0.700 CausalMutation CLINVAR Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. 17667967

2008
dbSNP: rs587776653
rs587776653
SDHC
T 0.700 GeneticVariation CLINVAR Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. 17667967

2008
dbSNP: rs764575966
rs764575966
SDHC
T 0.700 CausalMutation CLINVAR Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma. 17898811

2007
dbSNP: rs755235380
rs755235380
SDHC
G 0.700 CausalMutation CLINVAR Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. 16249420

2005
dbSNP: rs587776653
rs587776653
SDHC
T 0.700 GeneticVariation CLINVAR An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. 15342702

2004
dbSNP: rs587776653
rs587776653
SDHC
T 0.700 GeneticVariation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451

2003
dbSNP: rs587776653
rs587776653
SDHC
C 0.700 GeneticVariation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451

2003
dbSNP: rs587776652
rs587776652
SDHC
A 0.700 CausalMutation CLINVAR Mutations in SDHC cause autosomal dominant paraganglioma, type 3. 11062460

2000
dbSNP: rs755235380
rs755235380
SDHC
G 0.700 CausalMutation CLINVAR Mutations in SDHC cause autosomal dominant paraganglioma, type 3. 11062460

2000
dbSNP: rs1553264218
rs1553264218
SDHC
C 0.700 CausalMutation CLINVAR

dbSNP: rs1558182956
rs1558182956
SDHC
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587776653
rs587776653
SDHC
T 0.700 CausalMutation CLINVAR