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: rs1131692245
rs1131692245
7 0.925 0.160 19 35844109 missense variant C/T snv 0.700 0
dbSNP: rs1175052474
rs1175052474
5 1.000 2 227295295 inframe insertion -/AGG delins 7.0E-06 0.700 0
dbSNP: rs1272948499
rs1272948499
3 0.925 0.080 1 179575709 frameshift variant C/- delins 1.4E-05 0.700 0
dbSNP: rs138924661
rs138924661
9 0.807 0.120 17 56848773 stop gained G/A snv 9.1E-05 1.5E-04 0.700 0
dbSNP: rs1556411578
rs1556411578
4 X 108595507 coding sequence variant AAGGTGACA/- delins 0.700 0
dbSNP: rs1556445736
rs1556445736
5 0.925 0.200 X 108667167 synonymous variant A/G snv 0.700 0
dbSNP: rs1556463583
rs1556463583
2 X 108695350 frameshift variant -/A delins 0.700 0
dbSNP: rs199840952
rs199840952
7 0.827 0.240 2 97732893 missense variant C/T snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs267602852
rs267602852
WT1
7 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
dbSNP: rs281874674
rs281874674
8 0.827 0.280 X 108597479 missense variant G/C;T snv 0.700 0
dbSNP: rs530391015
rs530391015
5 0.882 0.080 14 104703445 stop gained G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs533297350
rs533297350
5 1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 0.700 0
dbSNP: rs569681869
rs569681869
6 0.925 0.040 2 227059468 missense variant C/G snv 7.2E-05 3.5E-05 0.700 0
dbSNP: rs779593707
rs779593707
2 1 16049884 stop gained -/AATA delins 1.2E-05 7.0E-06 0.700 0
dbSNP: rs869025224
rs869025224
7 0.827 0.240 2 97734709 missense variant G/C snv 7.0E-06 0.700 0
dbSNP: rs869025495
rs869025495
6 0.851 0.080 1 179564715 missense variant G/A snv 0.700 1.000 5 2004 2007
dbSNP: rs1428826948
rs1428826948
3 0.925 0.040 22 36265940 synonymous variant T/G snv 1.2E-05 0.700 1.000 1 2010 2010
dbSNP: rs1569534160
rs1569534160
3 0.925 0.040 22 36265812 missense variant A/G snv 0.700 1.000 1 2010 2010
dbSNP: rs2075252
rs2075252
5 0.925 0.160 2 169154475 stop gained T/A;C snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs74375025
rs74375025
3 1.000 0.040 10 16905665 intron variant G/A snv 8.1E-02 0.700 1.000 1 2019 2019