ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.835-11dup

dbSNP: rs201780112
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 RCV002121063 SCV002446839 benign 46,XY sex reversal 6 2025-01-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002121063 SCV002807864 likely benign 46,XY sex reversal 6 2022-01-13 criteria provided, single submitter clinical testing

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