Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs12532
MSX1
0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs3178250
BMP2
0.827 0.080 20 6779554 3 prime UTR variant T/C snv 0.21 5
rs8049367 0.851 0.240 16 3930444 downstream gene variant T/C snv 0.37 4
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
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
rs861019
IRF6
0.925 0.120 1 209802041 splice region variant A/G snv 0.44 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
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
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
rs7802
IRF6 ; C1orf74
1.000 1 209785814 3 prime UTR variant A/G snv 7.0E-04 1
rs758420403
EVC2
1.000 4 5689210 missense variant A/C snv 4.0E-06 1
rs104894562
FOXN1
0.882 0.200 17 28529157 stop gained C/T snv 4.0E-06 7.0E-06 3
rs1315861554
TGIF1
0.925 0.120 18 3457392 missense variant C/T snv 4.0E-06 2
rs116998555
WNT10A
0.882 0.080 2 218890118 missense variant C/A;T snv 4.0E-06; 1.9E-03 3
rs104894469
LOC105370455 ; PAX9
0.925 0.080 14 36663043 missense variant G/A;T snv 4.0E-06 2