ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.576C>T (p.Thr192=)

gnomAD frequency: 0.00017  dbSNP: rs372106846
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002099090 SCV002433837 likely benign 46,XY sex reversal 6 2024-09-14 criteria provided, single submitter clinical testing

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