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

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 13q31.3(chr13:92065660-92299019)x1
GRCh37/hg19 16q24.3(chr16:89689822-89726926)x3
GRCh37/hg19 19p13.3(chr19:4981959-5129575)x1
GRCh37/hg19 20p12.3(chr20:7103757-8075977)x3
GRCh37/hg19 2q36.3-37.1(chr2:230411764-232019784)x1
GRCh37/hg19 6q22.31(chr6:118767972-119044197)x3
GRCh37/hg19 9p24.3(chr9:691104-1063787)x1

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