ClinVar Miner

List of variants reported as pathogenic for Intellectual disability, autosomal dominant 13 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10031G>A (p.Arg3344Gln)	rs397509412
NM_001376.5(DYNC1H1):c.10975dup (p.Arg3659fs)
NM_001376.5(DYNC1H1):c.4700G>A (p.Arg1567Gln)	rs797044901

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