ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.1613A>G (p.Asn538Ser)

gnomAD frequency: 0.00001  dbSNP: rs374113323
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 RCV001034463 SCV001197820 likely benign 46,XY sex reversal 6 2019-08-27 criteria provided, single submitter clinical testing

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