Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs929387
GLI3
0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs116998555
WNT10A
0.882 0.080 2 218890118 missense variant C/A;T snv 4.0E-06; 1.9E-03 3
rs771803303
TGM2
0.882 0.160 20 38148005 missense variant G/A;C;T snv 1.6E-05; 4.1E-06 3
rs104894469
LOC105370455 ; PAX9
0.925 0.080 14 36663043 missense variant G/A;T snv 4.0E-06 2
rs1315861554
TGIF1
0.925 0.120 18 3457392 missense variant C/T snv 4.0E-06 2
rs140920120
BMP4
0.925 0.080 14 53952099 missense variant C/A;G snv 2.8E-04 2
rs28933970
PAX9 ; LOC105370455
0.925 0.080 14 36662954 missense variant T/C snv 2
rs483352804
EDA
0.925 0.080 X 70035389 missense variant G/A;T snv 2
rs1444216093
EVC2
1.000 4 5632031 missense variant G/A;C snv 1
rs15705
BMP2
1.000 20 6779333 3 prime UTR variant A/C;T snv 1
rs17015215
IRF6
1.000 1 209790735 missense variant C/T snv 1
rs758420403
EVC2
1.000 4 5689210 missense variant A/C snv 4.0E-06 1
rs777307167
WNT10A
1.000 2 218890128 missense variant T/C snv 1.2E-05 1
rs1292564852
FGFR3
1.000 4 1805414 missense variant C/T snv 7.0E-06 1
rs104894562
FOXN1
0.882 0.200 17 28529157 stop gained C/T snv 4.0E-06 7.0E-06 3
rs752627281
FGFR1
1.000 8 38419631 missense variant C/T snv 2.4E-05 6.3E-05 1
rs994158401
MSX1
1.000 4 4860050 missense variant A/G snv 1.4E-03 1.7E-04 1
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs7802
IRF6 ; C1orf74
1.000 1 209785814 3 prime UTR variant A/G snv 7.0E-04 1
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs1095
MSX1
0.925 0.080 4 4863211 3 prime UTR variant C/T snv 1.5E-02 2