Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776652
rs587776652
SDHC
A 0.700 CausalMutation CLINVAR Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3. 22351710

2012
dbSNP: rs587776652
rs587776652
SDHC
A 0.700 CausalMutation CLINVAR Mutations in SDHC cause autosomal dominant paraganglioma, type 3. 11062460

2000