List of variants reported as likely benign for VACTERL/vater association by Reutter Lab, Institute of Human Genetics, University Hospital Bonn

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 10q25.1(chr10:107722094-109081424)x3
GRCh37/hg19 12q23.1(chr12:100367541-100489446)x1
GRCh37/hg19 13q14.11(chr13:43505151-43762719)x3
GRCh37/hg19 13q31.3(chr13:93377562-93606814)x1
GRCh37/hg19 13q32.3-33.1(chr13:101605129-101748121)x1
GRCh37/hg19 15q25.2-25.3(chr15:84931022-85728834)x1
GRCh37/hg19 17p13.3(chr17:1007540-1254875)x3
GRCh37/hg19 17q25.3(chr17:80881583-81060040)x3
GRCh37/hg19 1q44(chr1:245900039-246475061)x1
GRCh37/hg19 2q21.1(chr2:132140614-132312325)x3
GRCh37/hg19 4q13.3(chr4:75720151-75883784)x1
GRCh37/hg19 5q22.1(chr5:111241351-111390356)x1
GRCh37/hg19 7p21.2(chr7:15424383-15534832)x3
GRCh37/hg19 7q35(chr7:147516080-147803861)x1
GRCh37/hg19 9q22.32(chr9:97290466-97419146)x1

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