ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.2824ACA[7] (p.Thr949del)

dbSNP: rs5868032
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502779 SCV000595698 benign not specified 2016-04-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000624971 SCV001726231 benign 46,XY sex reversal 6 2025-02-03 criteria provided, single submitter clinical testing

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