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: rs1057519726
rs1057519726
1 1.000 0.040 13 28018502 missense variant T/A;C;G snv 0.700 1.000 9 2005 2013
dbSNP: rs1057519745
rs1057519745
WT1
1 1.000 0.040 11 32396363 frameshift variant -/ACCGTACA ins 0.700 1.000 6 2014 2014
dbSNP: rs28931590
rs28931590
1 1.000 0.040 19 33302164 missense variant T/A snv 0.800 1.000 5 2001 2013
dbSNP: rs376588714
rs376588714
1 1.000 0.040 13 28018483 missense variant T/C snv 2.4E-05 1.4E-05 0.710 1.000 4 2005 2014
dbSNP: rs1057519749
rs1057519749
1 1.000 0.040 21 34880579 missense variant C/A;G snv 0.700 1.000 3 2014 2014
dbSNP: rs1057519762
rs1057519762
1 1.000 0.040 13 28018484 missense variant A/G snv 0.700 1.000 3 2012 2014
dbSNP: rs1057519765
rs1057519765
1 1.000 0.040 13 28027236 missense variant T/A;C snv 4.0E-06 0.700 1.000 3 2012 2014
dbSNP: rs1057519767
rs1057519767
1 1.000 0.040 13 28028205 missense variant T/C snv 0.700 1.000 3 2012 2014
dbSNP: rs1057519768
rs1057519768
1 1.000 0.040 13 28028279 missense variant T/C snv 0.700 1.000 3 2012 2014
dbSNP: rs1057519769
rs1057519769
1 1.000 0.040 13 28033974 missense variant C/A snv 0.700 1.000 3 2012 2014
dbSNP: rs1042919
rs1042919
1 1.000 0.040 11 4138534 3 prime UTR variant A/T snv 0.88 0.020 1.000 2 2013 2017
dbSNP: rs1057519750
rs1057519750
1 1.000 0.040 21 34880580 missense variant C/T snv 0.700 1.000 2 2009 2014
dbSNP: rs1057519764
rs1057519764
1 1.000 0.040 13 28027222 missense variant A/C;T snv 0.710 1.000 2 2012 2019
dbSNP: rs754921650
rs754921650
1 1.000 0.040 3 47120446 missense variant T/C snv 1.2E-05 2.1E-05 0.700 1.000 2 2005 2014
dbSNP: rs771684063
rs771684063
1 1.000 0.040 6 30665559 missense variant G/A;C snv 1.6E-05 0.020 1.000 2 2017 2019
dbSNP: rs10000770
rs10000770
1 1.000 0.040 4 142693109 intron variant C/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs10001414
rs10001414
1 1.000 0.040 4 168569930 intron variant A/G snv 1.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs10002854
rs10002854
1 1.000 0.040 4 7519419 intron variant C/T snv 8.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs10004892
rs10004892
1 1.000 0.040 4 188951696 intergenic variant T/C snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs10006108
rs10006108
1 1.000 0.040 4 97002862 intergenic variant C/T snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs10006418
rs10006418
1 1.000 0.040 4 142691588 intron variant A/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs10010954
rs10010954
1 1.000 0.040 4 150324302 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10011263
rs10011263
1 1.000 0.040 4 112807837 intergenic variant G/A snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs10012488
rs10012488
1 1.000 0.040 4 142671933 intron variant C/T snv 7.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs10019259
rs10019259
1 1.000 0.040 4 95825984 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017