List of variants reported as uncertain significance for See cases by ISCA site 3

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 16p13.2-13.13(chr16:10012281-10426437)x3
GRCh38/hg38 17q25.3(chr17:82911614-83048826)x1
GRCh38/hg38 1p35.2(chr1:30116821-30696608)x1
GRCh38/hg38 2q22.1(chr2:139896665-140201444)x3
GRCh38/hg38 3p26.3(chr3:190587-608819)x1
GRCh38/hg38 4q22.1(chr4:91475388-92263153)x3
GRCh38/hg38 7q22.3-31.1(chr7:105575647-107949294)x1
GRCh38/hg38 9p24.3(chr9:204104-343954)x3

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