ClinVar Miner

List of variants reported as likely pathogenic for chromosome 15q11.2 deletion syndrome

Included ClinVar conditions (1):

Chromosome 15q11.2 deletion syndrome

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000017.11:g.2688360_2784321del

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