ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.633+815T>C

dbSNP: rs1017226
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002122792 SCV002404005 benign 46,XY sex reversal 6 2024-11-05 criteria provided, single submitter clinical testing

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