ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.930A>C (p.Gly310=)

dbSNP: rs1579402124
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001504224 SCV001709096 likely benign Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2021-04-04 criteria provided, single submitter clinical testing

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