Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs17197936 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 3
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7033979
ASPN ; CENPP
0.925 0.040 9 92461698 intron variant A/G;T snv 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs6074028
CD40
1.000 0.040 20 46126219 intron variant A/C;G snv 1
rs73115010
CD40
1.000 0.040 20 46124597 intron variant T/C snv 0.18 1
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs1057519090
COL4A2
0.851 0.160 13 110492105 missense variant G/A snv 7
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1385889785
FCRL3
1.000 0.040 1 157695436 missense variant G/C;T snv 4.0E-06; 4.0E-06 2
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs204989
GPSM3
0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25