List of variants reported as uncertain significance by Centro Nacional de Genética Medica "Dr. Eduardo E. Castilla", Administración Nacional de Laboratorios e Institutos de Salud

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 11p15.4(chr11:6851550-6984119)x1
GRCh37/hg19 17p12(chr17:12895843-12921307)x3
GRCh37/hg19 19q13.42-13.43(chr19:55434660-56463734)x1
GRCh37/hg19 20p13(chr20:489033-898472)x3
GRCh37/hg19 3p26.3(chr3:1125700-1197682)x1
GRCh37/hg19 4p16.3(chr4:703668-869177)x3
GRCh37/hg19 4q13.3(chr4:73694233-73984429)x3
GRCh37/hg19 5q15(chr5:94478206-94864722)x1
GRCh37/hg19 9p24.3(chr9:204193-349093)x3
GRCh37/hg19 9p24.3(chr9:211086-416351)x3
GRCh37/hg19 Xp22.33(chrX:352586-599091)x3
GRCh37/hg19 Xp22.33(chrX:500243-699424)x3
GRCh37/hg19 Xp22.33(chrX:781241-1224296)x3
GRCh37/hg19 Xp22.33(chrX:781817-1232910)x3

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