List of variants reported as uncertain significance for See cases by ISCA site 7

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		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 13q32.1(chr13:95105459-95389895)x1
GRCh38/hg38 16q22.1(chr16:68937032-69254118)x3
GRCh38/hg38 16q23.1(chr16:77613187-78311038)x3
GRCh38/hg38 17p13.1-12(chr17:10713492-11312542)x3
GRCh38/hg38 1q42.3(chr1:234802578-235914149)x3
GRCh38/hg38 21q21.1-21.2(chr21:21843375-23953080)x1
GRCh38/hg38 8p23.2(chr8:2605460-2936937)x3
GRCh38/hg38 Xq27.2(chrX:141258990-141527921)x0

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