List of variants reported as uncertain significance for not provided by Institute of Human Genetics, University of Goettingen

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 11q14.1(chr11:83996454-84055732)x1
GRCh37/hg19 15q15.3(chr15:43888927-43933733)x1
GRCh37/hg19 16p13.13-13.12(chr16:12389767-13081111)x3
GRCh37/hg19 1p34.1(chr1:45923445-46017520)x1
GRCh37/hg19 20q13.12(chr20:45756621-45846429)x3
GRCh37/hg19 2q37.3(chr2:238245132-239052675)x3
GRCh37/hg19 5q13.1-13.2(chr5:68278453-70369959)x3
GRCh37/hg19 8q24.3(chr8:140893978-141050020)x3

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