Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 9
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1801208
WFS1
0.882 0.360 4 6301162 missense variant G/A snv 5.7E-02 5.0E-02 4
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 7
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs4821112
UBE2L3
22 21610472 intron variant G/A snv 0.21 4
rs140490
UBE2L3
1.000 0.080 22 21567397 intron variant G/A;C;T snv 2
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs55882956
TYK2
19 10359243 missense variant G/A;C snv 7.2E-03; 4.1E-06 1
rs3838646
TTTY14
0.827 0.320 Y 18991182 intron variant CA/- del 8
rs52812045
TTTY14
0.851 0.240 Y 18992540 non coding transcript exon variant G/A snv 7
rs8734
TTTY14
Y 18992540 non coding transcript exon variant G/A snv 1
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3