ClinVar Miner

Submissions for variant NM_001172509.2(SATB2):c.1861A>T (p.Ile621Phe)

dbSNP: rs1692190479
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Center for Mendelian Genomics, University of Washington RCV001291383 SCV001479857 likely pathogenic Autism spectrum disorder no assertion criteria provided research

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