ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.3846T>G (p.Ser1282=)

dbSNP: rs375842337
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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 RCV001466805 SCV001670816 likely benign 46,XY sex reversal 6 2019-02-05 criteria provided, single submitter clinical testing

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