Variants with conflicting interpretations "benign" from ISCA site 8 and "uncertain significance" from any submitter

Minimum review status of the submission from ISCA site 8:		Collection method of the submission from ISCA site 8:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 11q22.1(chr11:97849768-98439058)x1
GRCh38/hg38 15q11.2(chr15:22726969-23066575)x3
GRCh38/hg38 17p13.2(chr17:3640170-3656795)x1
GRCh38/hg38 1q21.1(chr1:145439580-147036021)x3
GRCh38/hg38 1q21.3(chr1:153641117-153752390)x3
GRCh38/hg38 2p11.2(chr2:87148954-87655401)x3
GRCh38/hg38 2p11.2(chr2:87148954-87705899)x3
GRCh38/hg38 2q13(chr2:110104900-110201550)x1
GRCh38/hg38 8q11.1(chr8:46031334-46662449)x1
GRCh38/hg38 Yq11.222(chrY:17251756-19149935)x2

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