ClinVar Miner

Submissions for variant NM_002830.4(PTPN4):c.2491C>A (p.Leu831Ile)

dbSNP: rs1679434397
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001256105 SCV001432892 uncertain significance Autism; Intellectual disability 2020-02-06 criteria provided, single submitter clinical testing

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