ClinVar Miner

Submissions for variant NM_003486.7(SLC7A5):c.737C>T (p.Ala246Val)

dbSNP: rs2143738378
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Yale Center for Mendelian Genomics, Yale University RCV001849610 SCV002106502 uncertain significance Autism spectrum disorder 2016-12-01 no assertion criteria provided literature only

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