ClinVar Miner

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

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NC_000005.9:g.136320037_136380192dup
NC_000010.10:g.102928083_103377947dup
Single allele

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