Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1567755946
AXIN2
0.925 0.080 17 65537563 frameshift variant -/CGCGGGAGGCAGC delins 2
rs752881223
AXIN2
0.925 0.080 17 65558307 missense variant A/C;G snv 2
rs1131692057
LOC105370455 ; PAX9
0.925 0.080 14 36662092 start lost G/A snv 2
rs754287422
LOC105370455 ; PAX9
0.925 0.080 14 36663308 missense variant A/G snv 2
rs34165410
MSX1
0.925 0.080 4 4860247 synonymous variant C/G;T snv 4.8E-06; 6.8E-02 2
rs515726227
MSX1
0.925 0.080 4 4863139 frameshift variant -/TA delins 2
rs7143727
PAX9
0.925 0.080 14 36666400 non coding transcript exon variant G/C snv 4.7E-02 2
rs779059411
PAX9
0.925 0.080 14 36666492 missense variant A/C;G snv 8.4E-06 2
rs374534090
PAX9 ; LOC105370455
0.925 0.080 14 36663506 missense variant G/A;C;T snv 4.2E-06; 4.2E-06 2
rs1392844787
ZNF569
0.925 0.080 19 37413765 missense variant T/C;G snv 4.0E-06; 4.0E-06 2
rs377467108
EZH2
0.882 0.120 7 148827254 missense variant C/A;T snv 6.4E-05 3
rs374910216
LOC107984111 ; WNT10A
0.882 0.080 2 218882358 missense variant G/A snv 2.4E-05 3
rs28933971
PAX9 ; LOC105370455
0.882 0.080 14 36662975 missense variant G/A;C snv 3
rs750190755
WNT10A
0.882 0.080 2 218893087 missense variant C/T snv 4.1E-05 7.0E-06 3
rs929387
GLI3
0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs1553763618
POLR3GL
0.925 0.040 1 145977482 splice acceptor variant G/A snv 4
rs782661984
POLR3GL
0.925 0.040 1 145974824 splice acceptor variant G/A snv 2.3E-05 1.4E-05 4
rs4904210
PAX9
0.851 0.080 14 36666548 missense variant G/C snv 0.36 0.33 5
rs730882193
AXIN2
0.807 0.200 17 65536472 stop gained C/G;T snv 6
rs775141057
LOC100287944 ; POLR3B
0.882 0.120 12 106496115 missense variant C/A;T snv 4.0E-06 2.1E-05 6
rs35822372 0.776 0.160 2 88438931 intergenic variant C/A;T snv 8
rs55846652 0.776 0.160 X 69564858 downstream gene variant T/C snv 0.29 8
rs917412 0.776 0.160 4 108350621 TF binding site variant C/T snv 0.21 8
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv 8
rs4498834
CACNA1S
0.776 0.160 1 201111170 intron variant T/C snv 0.56 8