Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs4693608
HPSE
0.827 0.200 4 83320204 intron variant G/A;C snv 6
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv 5
rs2881766
ESR1
0.882 0.120 6 151797984 intron variant T/G snv 0.35 5
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs2064863
AURKA
0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs2105269
GALNT16
0.882 0.120 14 69280517 intron variant A/G snv 0.35 4
rs3218038
CCNE1
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02 4
rs3748093
BRAF
0.925 0.120 7 140800651 intron variant T/A snv 1.5E-02 4
rs3917356
IL1B
0.882 0.160 2 112834786 intron variant C/T snv 0.39 4
rs6720283
COL6A3
0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs738722
CHEK2
0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs2253319
RUNX1
0.882 0.120 21 34815749 intron variant C/G;T snv 3
rs3801004
FSCN1
0.882 0.120 7 5598591 intron variant C/A;G;T snv 3
rs11600655
PLAAT3
0.925 0.120 11 63606853 intron variant G/C snv 0.27 2
rs7166348
IGF1R
1.000 0.080 15 98704566 intron variant G/A;T snv 0.21 2
rs8105637
TINCR
0.925 0.120 19 5566221 intron variant A/G snv 0.56 2
rs11581557
TRIT1
1.000 0.080 1 39862786 intron variant A/C;T snv 1
rs1190271
POPDC3
1.000 0.080 6 105176946 intron variant G/A;C snv 1
rs34904192
MIR155HG
1.000 0.080 21 25569623 intron variant G/A snv 0.12 1
rs7186053
CDH1
1.000 0.080 16 68805390 intron variant A/G snv 0.69 1
rs17530068
LOC105377871
0.882 0.120 6 81483392 intergenic variant T/C snv 0.19 3
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11