ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.233_234delinsCT (p.Leu78Pro)

dbSNP: rs1554028405
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000648706 SCV000770527 benign 46,XY sex reversal 6 2024-11-19 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001816609 SCV002069680 benign not specified 2021-02-23 criteria provided, single submitter clinical testing

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