ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.*133G>C (rs193112615)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000334630 SCV000457073 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000379866 SCV000457074 uncertain significance Mitochondrial complex II deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000285270 SCV000457075 uncertain significance Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing

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