List of intergenic variants reported as uncertain significance for adenocarcinoma

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: 3

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 1p36.11(chr1:26519016-26520363)x0
GRCh38/hg38 1p36.21(chr1:13272807-13275727)x1
NC_000005.10:g.101281019_101281030del

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