ClinVar Miner

Submissions for variant NM_004168.3(SDHA):c.-115T>C

gnomAD frequency: 0.25160  dbSNP: rs2303741
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000338764 SCV000456953 likely benign Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000400671 SCV000456954 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000313041 SCV000456955 likely benign Mitochondrial complex II deficiency, nuclear type 1 2016-06-14 criteria provided, single submitter clinical testing

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