ClinVar Miner

Submissions for variant NM_005006.7(NDUFS1):c.1299C>T (p.Gly433=)

dbSNP: rs2105961351
Minimum review status: Collection method:
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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 RCV002047656 SCV002288870 uncertain significance not provided 2021-08-28 criteria provided, single submitter clinical testing

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