Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039792
TXNDC15
0.807 0.280 5 134874531 splice donor variant G/A snv 9
rs767978562
FREM2
0.790 0.320 13 38851093 stop gained C/T snv 8.0E-06 7.0E-06 8
rs9332967
SRD5A2
0.790 0.200 2 31526224 missense variant C/T snv 2.3E-04 1.1E-04 7
rs267602852
WT1
0.827 0.160 11 32417631 missense variant G/A snv 7
rs122445099
ATRX
0.827 0.400 X 77520832 stop gained G/A snv 6
rs1565286228
MYRF
0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 6
rs2234584
WT1
0.882 0.240 11 32428521 missense variant G/A;T snv 3.9E-04; 2.8E-05 5
rs1800053
AR
0.851 0.160 X 67711453 missense variant C/A snv 1.1E-03 1.2E-03 4
rs104894136
CYP17A1-AS1 ; WBP1L ; CYP17A1
0.882 0.200 10 102834074 stop gained G/A snv 4
rs137852567
AR
0.882 0.200 X 67717595 missense variant A/G snv 3
rs104894061
CYP11B1 ; GML
0.882 0.200 8 142876242 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 3
rs104894137
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.882 0.200 10 102832626 missense variant G/T snv 3
rs137852592
AR
0.925 0.160 X 67721937 missense variant T/C snv 2
rs142647336
HSD3B1
1.000 0.160 1 119514302 missense variant C/A;T snv 4.0E-05 1.0E-04 1