ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.622-7C>T

dbSNP: rs759371428
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000951952 SCV001098409 likely benign Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2023-12-06 criteria provided, single submitter clinical testing
Mendelics RCV000987494 SCV001136797 likely benign Mitochondrial complex II deficiency, nuclear type 1 2019-05-28 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003736943 SCV004563117 likely benign not provided 2023-09-06 criteria provided, single submitter clinical testing

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