ClinVar Miner

List of variants reported as uncertain significance for Intellectual disability, autosomal dominant 13 by MGZ Medical Genetics Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10070A>G (p.Glu3357Gly)	rs1458996905	0.00001
NM_001376.5(DYNC1H1):c.10549G>A (p.Ala3517Thr)	rs2152592178
NM_001376.5(DYNC1H1):c.6058C>G (p.Pro2020Ala)	rs2503750846

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