Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 4
rs314313
EPHB4 ; SLC12A9
1.000 0.040 7 100825743 intron variant T/A;C;G snv 0.29 2
rs34688635
NOX1
X 100850206 missense variant C/T snv 1.9E-02 2.0E-02 1
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs503734
IMPG2
1.000 0.040 3 101304904 intron variant A/G snv 0.40 2
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 3
rs1420098
IL18R1
2 102367819 splice region variant T/C snv 0.35 0.33 1
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs6708413
IL18RAP
1.000 0.040 2 102446909 intron variant G/A snv 0.78 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2274351
SUFU ; ACTR1A
10 102504350 intron variant C/G;T snv 0.48 1
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs1426809883
ICAM1
19 10284797 missense variant G/A snv 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
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
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs11879191
CDC37
1.000 0.040 19 10402235 intron variant G/A;C snv 2
rs35164067
CDC37
1.000 0.040 19 10414505 intron variant G/A snv 0.18 2
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs6568421 1.000 0.040 6 105987150 regulatory region variant A/G snv 0.23 2
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5