List of variants reported as uncertain significance for Neurodevelopmental disorder by Rare Disease Group, Clinical Genetics, Karolinska Institutet

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NC_000005.9:g.53180658_54552379dup
NC_000007.13:g.30439214_30632407dup
NC_000009.11:g.6558199_6619973dup
NC_000018.9:g.67742689_67765169dup
NC_000019.9:g.1406030_3597207dup
NC_000020.10:g.157772_706326dup
Single allele

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