Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758420403
EVC2
1.000 4 5689210 missense variant A/C snv 4.0E-06 1
rs15705
BMP2
1.000 20 6779333 3 prime UTR variant A/C;T snv 1
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs17563
BMP4
0.790 0.320 14 53950804 stop lost A/G snv 0.45 0.44 8
rs861019
IRF6
0.925 0.120 1 209802041 splice region variant A/G snv 0.44 2
rs7802
IRF6 ; C1orf74
1.000 1 209785814 3 prime UTR variant A/G snv 7.0E-04 1
rs994158401
MSX1
1.000 4 4860050 missense variant A/G snv 1.4E-03 1.7E-04 1
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs140920120
BMP4
0.925 0.080 14 53952099 missense variant C/A;G snv 2.8E-04 2
rs116998555
WNT10A
0.882 0.080 2 218890118 missense variant C/A;T snv 4.0E-06; 1.9E-03 3
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs2235371
IRF6
0.752 0.360 1 209790735 missense variant C/T snv 8.7E-02 3.9E-02 11
rs8670
MSX1
0.925 0.080 4 4863149 3 prime UTR variant C/T snv 0.22 0.23 4
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
rs1315861554
TGIF1
0.925 0.120 18 3457392 missense variant C/T snv 4.0E-06 2
rs114632254
EDARADD
1.000 1 236482309 missense variant C/T snv 2.1E-02 2.1E-02 1
rs1292564852
FGFR3
1.000 4 1805414 missense variant C/T snv 7.0E-06 1
rs17015215
IRF6
1.000 1 209790735 missense variant C/T snv 1