ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.1644A>G (p.Gln548=)

gnomAD frequency: 0.02279  dbSNP: rs56225368
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 RCV000878120 SCV001020974 benign 46,XY sex reversal 6 2024-12-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717724 SCV005301120 benign not provided criteria provided, single submitter not provided

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