Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs11574311
WRN
0.776 0.160 8 31119144 intron variant T/C snv 0.16 8
rs2725338
WRN
0.790 0.120 8 31042501 intron variant G/A snv 7.6E-02 7
rs6596473
SLC23A1
0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs2725383
WRN
0.807 0.120 8 31075099 intron variant C/G snv 0.76 6
rs4733220
WRN
0.807 0.120 8 31043374 intron variant A/G snv 0.50 6
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs17175798
ANKRD34C-AS1
0.925 0.040 15 79171618 intron variant C/A;T snv 3
rs2101521
TLR1
0.925 0.080 4 38809930 intron variant G/A;T snv 3
rs11129182
RARB
0.925 0.120 3 25129806 intron variant T/C snv 0.82 2
rs17047586
TAFA1
0.925 0.120 3 68363724 intron variant A/G snv 8.6E-03 2
rs8007903
KLC1
0.925 0.120 14 103671306 intron variant A/G snv 0.27 2
rs4613984
IDO1
1.000 0.040 8 39919023 intron variant G/A;T snv 3.9E-02; 8.2E-06 1
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs11260867 1.000 0.040 1 16115233 regulatory region variant C/G snv 0.13 1
rs7543472 1.000 0.040 1 16113897 regulatory region variant C/A;G;T snv 1
rs1057518802
SLC19A1 ; COL18A1
0.882 0.080 21 45509554 stop gained C/T snv 4
rs1303044966
ABHD12
0.882 0.160 20 25339294 stop gained G/A;C snv 4.0E-06 4
rs398122944
LOC100507443 ; CRYGC
0.851 0.200 2 208128257 stop gained C/G;T snv 4
rs121909598
CRYGD ; LOC100507443
0.882 0.040 2 208121728 stop gained C/T snv 4.0E-06 3
rs398122392
CRYGC ; LOC100507443
0.882 0.040 2 208128258 stop gained C/A;G;T snv 2.4E-05; 8.0E-06 3
rs140372256
CRYGA
0.925 0.040 2 208160859 stop gained C/A;G;T snv 1.5E-04; 1.6E-05; 4.0E-06 2