Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555913934
rs1555913934
1 1.000 0.160 22 28695868 frameshift variant AG/- del 0.700 1.000 22 1999 2014
dbSNP: rs10060683
rs10060683
1 1.000 0.160 5 92523322 intron variant T/C snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs1027643
rs1027643
1 1.000 0.160 5 92558085 intron variant C/T snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs10767935
rs10767935
WT1
1 1.000 0.160 11 32405158 intron variant C/T snv 0.27 0.010 1.000 1 2015 2015
dbSNP: rs11913239
rs11913239
1 1.000 0.160 22 30613852 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs16988855
rs16988855
1 1.000 0.160 22 30615936 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs2009857
rs2009857
1 1.000 0.160 22 30618390 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2221269
rs2221269
1 1.000 0.160 5 92571299 intron variant A/G snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs2234590
rs2234590
WT1
1 1.000 0.160 11 32399987 synonymous variant T/C snv 1.2E-02 4.6E-02 0.010 1.000 1 2005 2005
dbSNP: rs2267166
rs2267166
1 1.000 0.160 22 30622091 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs2283873
rs2283873
1 1.000 0.160 22 30617309 intron variant G/A snv 8.8E-02 0.12 0.800 1.000 1 2012 2012
dbSNP: rs2495478
rs2495478
1 1.000 0.160 1 55047322 non coding transcript exon variant G/A snv 0.13 0.800 1.000 1 2012 2012
dbSNP: rs3755132
rs3755132
1 1.000 0.160 2 15589696 upstream gene variant T/G snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs5030244
rs5030244
WT1
1 1.000 0.160 11 32402206 intron variant T/C snv 4.6E-02 0.010 1.000 1 2015 2015
dbSNP: rs5955543
rs5955543
NHS
1 1.000 0.160 X 17680277 intron variant A/G snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs61344503
rs61344503
1 1.000 0.160 5 92568740 intron variant G/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs6887553
rs6887553
1 1.000 0.160 5 92510102 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs7288385
rs7288385
1 1.000 0.160 22 30619586 intron variant C/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs7288627
rs7288627
1 1.000 0.160 22 30619575 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs7290898
rs7290898
1 1.000 0.160 22 30615293 splice region variant A/C;G;T snv 7.9E-02; 2.9E-04; 1.1E-03 0.700 1.000 1 2012 2012
dbSNP: rs7585356
rs7585356
1 1.000 0.160 2 214727582 3 prime UTR variant G/A snv 0.27 0.010 1.000 1 2017 2017
dbSNP: rs776031963
rs776031963
1 1.000 0.160 9 123371433 missense variant G/A snv 2.0E-05 2.1E-05 0.010 1.000 1 2019 2019
dbSNP: rs790356
rs790356
1 1.000 0.160 11 83909744 intron variant A/G snv 0.50 0.800 1.000 1 2012 2012
dbSNP: rs8141515
rs8141515
1 1.000 0.160 22 30622085 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs1131690795
rs1131690795
1 1.000 0.160 11 32434769 frameshift variant C/- delins 0.700 0