Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894469
LOC105370455 ; PAX9
0.925 0.080 14 36663043 missense variant G/A;T snv 4.0E-06 2
rs104894562
FOXN1
0.882 0.200 17 28529157 stop gained C/T snv 4.0E-06 7.0E-06 3
rs1095
MSX1
0.925 0.080 4 4863211 3 prime UTR variant C/T snv 1.5E-02 2
rs11001553
PRKG1-AS1 ; DKK1
0.925 0.080 10 52313141 intron variant C/T snv 0.12 2
rs114632254
EDARADD
1.000 1 236482309 missense variant C/T snv 2.1E-02 2.1E-02 1
rs116998555
WNT10A
0.882 0.080 2 218890118 missense variant C/A;T snv 4.0E-06; 1.9E-03 3
rs11806449
GREM2
1.000 1 240493497 intron variant G/A snv 0.21 0.17 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
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs1292564852
FGFR3
1.000 4 1805414 missense variant C/T snv 7.0E-06 1
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
rs1444216093
EVC2
1.000 4 5632031 missense variant G/A;C snv 1
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
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
rs17563
BMP4
0.790 0.320 14 53950804 stop lost A/G snv 0.45 0.44 8
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs2235371
IRF6
0.752 0.360 1 209790735 missense variant C/T snv 8.7E-02 3.9E-02 11
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13