ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.1566C>T (p.Thr522=)

gnomAD frequency: 0.04382  dbSNP: rs2229882
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000550395 SCV000650500 benign 46,XY sex reversal 6 2025-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001672842 SCV001887502 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001672842 SCV005301119 benign not provided criteria provided, single submitter not provided

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