Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202101384
rs202101384
SDHB
A 0.700 GeneticVariation CLINVAR Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling. 27604842

2017
dbSNP: rs202101384
rs202101384
SDHB
A 0.700 GeneticVariation CLINVAR Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy. 26642834

2016
dbSNP: rs202101384
rs202101384
SDHB
A 0.700 GeneticVariation CLINVAR Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance. 26925370

2015
dbSNP: rs202101384
rs202101384
SDHB
A 0.700 GeneticVariation CLINVAR Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. 22972948

2012