Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519389
EBF3
0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs1131692034
EDA
0.790 0.160 X 69616488 stop gained C/A snv 14
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs797044484
TP63
0.776 0.400 3 189868624 missense variant C/G snv 10
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs35822372 0.776 0.160 2 88438931 intergenic variant C/A;T snv 8
rs55846652 0.776 0.160 X 69564858 downstream gene variant T/C snv 0.29 8
rs917412 0.776 0.160 4 108350621 TF binding site variant C/T snv 0.21 8
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv 8
rs4498834
CACNA1S
0.776 0.160 1 201111170 intron variant T/C snv 0.56 8
rs35956082
FOXP1
0.776 0.160 3 71414748 intron variant A/C;G snv 8
rs758468472
NOL11 ; LOC101928045
0.776 0.160 17 67718094 splice region variant G/T snv 8
rs730882193
AXIN2
0.807 0.200 17 65536472 stop gained C/G;T snv 6
rs67682641
COL1A1
0.807 0.240 17 50194375 missense variant C/A;T snv 6
rs4904210
PAX9
0.851 0.080 14 36666548 missense variant G/C snv 0.36 0.33 5
rs132630321
EDA
0.851 0.120 X 70035446 missense variant C/T snv 5.5E-06 9.6E-06 4
rs929387
GLI3
0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs142343894
GREM2
0.851 0.080 1 240493250 missense variant G/C snv 1.7E-03 1.8E-03 4
rs8670
MSX1
0.925 0.080 4 4863149 3 prime UTR variant C/T snv 0.22 0.23 4
rs377467108
EZH2
0.882 0.120 7 148827254 missense variant C/A;T snv 6.4E-05 3
rs121909637
FGFR1
0.882 0.240 8 38418249 missense variant C/A;T snv 1.2E-05; 2.0E-05 3
rs374910216
LOC107984111 ; WNT10A
0.882 0.080 2 218882358 missense variant G/A snv 2.4E-05 3