ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1795-66C>T

gnomAD frequency: 0.98913  dbSNP: rs387134
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001544166 SCV001763152 benign Dilated cardiomyopathy 1GG 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001544167 SCV001763153 benign Mitochondrial complex II deficiency, nuclear type 1 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001544302 SCV001763313 benign Neurodegeneration with ataxia and late-onset optic atrophy 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716760 SCV005302891 benign not provided criteria provided, single submitter not provided

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