List of intergenic variants reported as likely benign by Dept. Genetics and Cancer, Menzies Institute for Medical Research, University of Tasmania

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: 2

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HGVS	dbSNP	gnomAD frequency
NC_000001.11:g.239953380_239953381insGTGTGTGAGGCAGAGCCGGTGTGTGAGGAGGCCTGGGGGTGGGTTCATGTGAGCCCGTGGGGAGGGGACAGGGCTGGACTGCACAGAGCAGAGCTGCCAGAAGCTGAGGAGCGGACGCAGCAATGAGAAACTCAGCCCAATCATGTGGCCGACTGCAGTCTGGAAGACTTCCTGGGTGTGGAGTTTCTCTGAGTTTCTCAGAAAGGCAGAGGGAAGATTTTTGTCAGTAGAAGGCACATGGAAAGTCAGTCATGTTAGTGATCTTTCCTCCTCTGGCAGCTCCAGAGCCAGCTCCAGTTCAAGCTCAAAAGCCACCTTCAGAGTGTGTGTCAGGGCTAGGTCCACCACCAGCTCCAGCTGCAGCCTTAACCACCAG	rs1274870693
NC_000003.12:g.176518923_176519268dup	rs2108347906

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