Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10519612
IL15
0.882 0.120 4 141732548 intron variant A/C snv 0.10 3
rs111978267
KCNQ1
0.882 0.120 11 2751648 intron variant C/G;T snv 2.8E-05 3
rs3731246
CDKN2A
0.882 0.120 9 21971990 intron variant C/G snv 0.11 3
rs3794012
LMO1
0.882 0.120 11 8248697 intron variant T/C snv 0.32 3
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs414580
MSR1
0.882 0.120 8 16177793 intron variant T/A;C snv 3
rs4237770
LMO1
0.882 0.120 11 8254288 intron variant T/C snv 0.37 3
rs442264
LMO1
0.882 0.120 11 8242602 intron variant G/A snv 0.44 3
rs4958351
GRIA1
0.882 0.120 5 153790814 intron variant G/A;T snv 0.31 3
rs525549
KMT2A
0.882 0.120 11 118487353 intron variant T/A snv 0.33 3
rs6461639
RAPGEF5
0.882 0.120 7 22147337 intron variant T/A;C snv 3
rs7039798
FPGS
0.882 0.120 9 127794947 intron variant G/A;C snv 3
rs7286979
EP300
0.882 0.120 22 41102623 intron variant G/A snv 0.26 3
rs7809758
DDC ; FIGNL1
0.882 0.120 7 50505635 intron variant A/G snv 0.36 3
rs880028
FIGNL1 ; DDC
0.882 0.120 7 50502438 intron variant A/G snv 0.21 3
rs17213693
HLA-DOB
0.925 0.120 6 32813344 intron variant G/C snv 9.8E-02 2
rs442767
MSH3 ; DHFR
0.925 0.120 5 80655677 intron variant G/T snv 0.27 2
rs7896246
ARID5B
0.925 0.120 10 61964631 intron variant A/G snv 0.74 2
rs886285
IRF1-AS1
0.925 0.120 5 132429514 intron variant T/C snv 0.57 2
rs10853104
IGF2BP1
1.000 0.120 17 49014714 intron variant C/G;T snv 1
rs72846714
NT5C2
1.000 0.120 10 103118697 intron variant G/A snv 0.15 1
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs78380171
LOC101927518
0.925 0.120 3 86720838 intergenic variant A/G snv 6.6E-03 2
rs76925697 0.925 0.120 9 81132456 regulatory region variant A/T snv 3.4E-02 2