ClinVar Miner

List of variants reported as uncertain significance for Intellectual disability, autosomal dominant 16 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003072.5(SMARCA4):c.1693A>G (p.Thr565Ala)	rs765974121
NM_003072.5(SMARCA4):c.2029G>A (p.Ala677Thr)	rs2088396631
NM_003072.5(SMARCA4):c.557C>G (p.Ala186Gly)

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