List of intergenic variants reported as benign by Cytogenetics Laboratory, University of Washington

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
GRCh37/hg19 13q21.33(chr13:71136977-71585455)x3
GRCh37/hg19 14q12(chr14:28062826-28192913)x1
GRCh37/hg19 Xp22.33(chrX:907817-1244544)x3

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