ClinVar Miner

Submissions for variant NM_005921.2(MAP3K1):c.1923G>A (p.Met641Ile)

dbSNP: rs886041049
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Shenzhen Institute of Pediatrics, Shenzhen Children's Hospital RCV000258799 SCV000328449 likely pathogenic 46,XY sex reversal 6 2015-03-13 no assertion criteria provided clinical testing

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