ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.5CGG[5] (p.Ala5dup)

dbSNP: rs779149827
Minimum review status: Collection method:
Minimum conflict level:
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 RCV002127471 SCV002401634 benign 46,XY sex reversal 6 2024-11-22 criteria provided, single submitter clinical testing
Mendelics RCV002246681 SCV002518678 benign not specified 2022-05-04 criteria provided, single submitter clinical testing

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