ClinVar Miner

Submissions for variant NM_004168.3(SDHA):c.-84dup

dbSNP: rs35805262
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000370159 SCV000456956 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000399941 SCV000456957 likely benign Mitochondrial complex II deficiency, nuclear type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000307350 SCV000456958 likely benign Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing

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