Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs929387
GLI3
0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs994158401
MSX1
1.000 4 4860050 missense variant A/G snv 1.4E-03 1.7E-04 1
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
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs11001553
PRKG1-AS1 ; DKK1
0.925 0.080 10 52313141 intron variant C/T snv 0.12 2
rs17563
BMP4
0.790 0.320 14 53950804 stop lost A/G snv 0.45 0.44 8
rs140920120
BMP4
0.925 0.080 14 53952099 missense variant C/A;G snv 2.8E-04 2
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
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
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs15705
BMP2
1.000 20 6779333 3 prime UTR variant A/C;T snv 1
rs3178250
BMP2
0.827 0.080 20 6779554 3 prime UTR variant T/C snv 0.21 5
rs483352804
EDA
0.925 0.080 X 70035389 missense variant G/A;T snv 2
rs2268626
IFT43 ; TGFB3
1.000 14 75978424 intron variant C/T snv 0.80 1
rs317250 1.000 2 76036546 intron variant C/T snv 0.96 1