ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.3087C>T (p.Phe1029=)

gnomAD frequency: 0.00373  dbSNP: rs146112116
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 RCV000878647 SCV001021583 benign 46,XY sex reversal 6 2023-12-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716626 SCV005301132 benign not provided criteria provided, single submitter not provided

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