Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1813443
CNTN5
1.000 0.040 11 100140279 intron variant G/A;C snv 1
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
rs1277073914
MUC12
0.925 0.040 7 100992117 missense variant T/A snv 2
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
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs34592089
BANK1
1.000 0.040 4 102005766 intron variant G/A;T snv 2
rs4851529
LOC107985926
0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 5
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 3
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
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
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs230534
NFKB1
0.882 0.120 4 102527884 intron variant T/C snv 0.73 3
rs7705924
LINC00492 ; LINC00491
1.000 0.040 5 102611094 intron variant A/G snv 5.1E-02 1
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38