ClinVar Miner

List of intergenic variants reported as uncertain significance for Intellectual disability, mild

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NCBI36/hg18 16q24.3(chr16:87891000-88572000)

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