Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2235371
IRF6
0.752 0.360 1 209790735 missense variant C/T snv 8.7E-02 3.9E-02 11
rs861019
IRF6
0.925 0.120 1 209802041 splice region variant A/G snv 0.44 2
rs114632254
EDARADD
1.000 1 236482309 missense variant C/T snv 2.1E-02 2.1E-02 1
rs11806449
GREM2
1.000 1 240493497 intron variant G/A snv 0.21 0.17 1
rs17015215
IRF6
1.000 1 209790735 missense variant C/T snv 1
rs7802
IRF6 ; C1orf74
1.000 1 209785814 3 prime UTR variant A/G snv 7.0E-04 1
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs116998555
WNT10A
0.882 0.080 2 218890118 missense variant C/A;T snv 4.0E-06; 1.9E-03 3
rs317250 1.000 2 76036546 intron variant C/T snv 0.96 1
rs777307167
WNT10A
1.000 2 218890128 missense variant T/C snv 1.2E-05 1
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs8670
MSX1
0.925 0.080 4 4863149 3 prime UTR variant C/T snv 0.22 0.23 4
rs1095
MSX1
0.925 0.080 4 4863211 3 prime UTR variant C/T snv 1.5E-02 2
rs1292564852
FGFR3
1.000 4 1805414 missense variant C/T snv 7.0E-06 1
rs1444216093
EVC2
1.000 4 5632031 missense variant G/A;C snv 1
rs758420403
EVC2
1.000 4 5689210 missense variant A/C snv 4.0E-06 1
rs994158401
MSX1
1.000 4 4860050 missense variant A/G snv 1.4E-03 1.7E-04 1
rs929387
GLI3
0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs752627281
FGFR1
1.000 8 38419631 missense variant C/T snv 2.4E-05 6.3E-05 1
rs61735045
COL5A1
0.882 0.160 9 134750808 missense variant G/A snv 3.5E-02 3.1E-02 3
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs11001553
PRKG1-AS1 ; DKK1
0.925 0.080 10 52313141 intron variant C/T snv 0.12 2