ClinVar Miner

Submissions for variant NM_001093.4(ACACB):c.1963A>G (p.Ser655Gly)

dbSNP: rs2044635183
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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 RCV001291444 SCV001479946 association Autism spectrum disorder no assertion criteria provided research

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