Variants with conflicting interpretations "uncertain significance" from ISCA site 1 and "likely benign" from Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum review status of the submission from ISCA site 1:		Collection method of the submission from ISCA site 1:
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: 7

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 13q21.2-21.31(chr13:61660181-63785757)x3
GRCh37/hg19 1p33(chr1:49498351-50440974)x1
GRCh37/hg19 2q21.1(chr2:130166042-130784390)x3
GRCh37/hg19 4q22.1(chr4:92491756-93233588)x3
GRCh37/hg19 4q32.3(chr4:164801123-165481802)x3
GRCh37/hg19 7p21.1(chr7:16838232-17753807)x3
GRCh37/hg19 Xq21.31(chrX:87837389-88164567)x1

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