Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758430171
ICAM1
1.000 0.120 19 10284840 missense variant C/G snv 4.3E-06 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs572527200
MMP12
0.882 0.240 11 102875064 upstream gene variant T/C snv 4
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs769283795
KLRD1
1.000 0.120 12 10313425 missense variant A/G;T snv 8.2E-06 1
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 6
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs39984
MACIR
1.000 0.120 5 103261591 intron variant G/T snv 0.30 1
rs2561477
MACIR
1.000 0.120 5 103273223 intron variant G/A snv 0.24 1
rs7258015
ICAM3
0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs1166916365
RNPC3
1.000 0.120 1 103546277 missense variant T/C snv 1
rs4918037
SH3PXD2A
1.000 0.120 10 103653282 intron variant A/G snv 0.88 1
rs750018164
KLRC1
1.000 0.120 12 10450529 missense variant A/G;T snv 4.0E-06; 2.0E-04 1
rs4264325
TMEM179
1.000 0.120 14 104513149 intron variant T/C snv 0.97 1
rs2841277
PLD4
0.882 0.120 14 104924668 upstream gene variant C/T snv 0.41 3
rs2582532
PLD4
1.000 0.120 14 104926500 intron variant T/C snv 0.93 1
rs9651713
CASP5
1.000 0.120 11 105004030 intron variant G/A snv 0.13 1
rs552217
CASP5
1.000 0.120 11 105009264 intron variant T/G snv 1
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7