ClinVar Miner

Submissions for variant NM_015570.4(AUTS2):c.857_858del (p.Lys286fs)

dbSNP: rs864321694
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000203570 SCV000258919 pathogenic Autism spectrum disorder due to AUTS2 deficiency 2015-06-01 no assertion criteria provided literature only

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