Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518764
DLX3
0.827 0.200 17 49991807 frameshift variant C/-;CC delins 6
rs1555617226
DLX3
0.851 0.160 17 49993440 missense variant C/A snv 4
rs1085307111
ACP4 ; LOC105372439
0.882 0.080 19 50793784 missense variant C/T snv 3
rs104894738
ARHGAP6 ; AMELX
0.882 0.080 X 11294799 missense variant G/C snv 3
rs1432600424
CNNM4
0.882 0.120 2 96799118 stop gained C/G;T snv 7.0E-06 3
rs546603773
LOC105372439 ; ACP4
0.882 0.080 19 50791780 missense variant C/A;G;T snv 8.3E-06; 8.3E-06; 5.4E-05 3
rs104894737
AMELX ; ARHGAP6
0.925 0.080 X 11294790 start lost T/C snv 2
rs1060499539
ENAM
0.925 0.080 4 70631707 missense variant T/G snv 2
rs144411158
FAM20A
0.925 0.200 17 68555742 stop gained G/A;T snv 4.4E-05; 4.0E-06 2
rs137854435
FAM83H
0.925 0.080 8 143728488 stop gained G/A snv 2
rs137854436
FAM83H
0.925 0.080 8 143728269 stop gained G/A snv 2
rs556734208
KLK4
0.925 0.080 19 50907067 frameshift variant A/- del 2.1E-04 2.8E-05 2
rs1553275070
LAMB3
0.925 0.080 1 209615408 splice acceptor variant C/T snv 2
rs1553275195
LAMB3
0.925 0.080 1 209616513 stop gained C/A snv 2
rs587777516
LOC101928477 ; MMP20
0.925 0.080 11 102625218 stop gained C/G;T snv 2.0E-05; 3.6E-05 2
rs61730849
LOC101928477 ; MMP20
0.925 0.080 11 102611889 missense variant G/A snv 1.5E-03 1.8E-03 2
rs1270453185
ACP4 ; LOC105372439
1.000 0.080 19 50795064 missense variant C/G snv 4.4E-06 1
rs747301994
COL17A1
1.000 0.080 10 104053097 stop gained G/A;T snv 8.0E-06 1
rs1171002040
FAM83H
1.000 0.080 8 143730578 missense variant G/C snv 1
rs140967203
ITGB6
1.000 0.080 2 160142065 missense variant C/T snv 6.7E-05 1.3E-04 1
rs61737764
ITGB6
1.000 0.080 2 160137782 missense variant C/T snv 8.0E-03 3.9E-03 1
rs779692470
ITGB6
1.000 0.080 2 160172592 missense variant C/T snv 2.8E-05 1
rs148040455
MMP25
1.000 0.080 16 3050532 missense variant C/A;G;T snv 5.0E-06 1
rs770804941
WDR72
1.000 0.080 15 53733062 stop gained G/A;C snv 2.4E-05; 3.6E-05 1