List of intergenic variants reported as uncertain significance by Institute of Human Genetics, University of Goettingen

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: 7

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 10q21.1(chr10:58932423-59272160)x1
GRCh37/hg19 11p14.1(chr11:30834034-30902723)x3
GRCh37/hg19 7p12.1(chr7:53757193-53836967)x0
GRCh37/hg19 7q36.2(chr7:154390339-154546335)x3
GRCh37/hg19 Xp22.32(chrX:5073112-5578094)x1
GRCh37/hg19 Xp22.33(chrX:498249-681607)x3
GRCh37/hg19 Xq22.1(chrX:98441030-98832991)x2

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