ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.3667-13G>A

gnomAD frequency: 0.08897  dbSNP: rs16886463
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001679581 SCV001904116 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073219 SCV002393114 benign 46,XY sex reversal 6 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001679581 SCV005301136 benign not provided criteria provided, single submitter not provided

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