Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs11045879
SLCO1B1
1.000 0.120 12 21229685 intron variant T/C snv 0.18 4
rs1883112
NCF4-AS1 ; NCF4
0.851 0.200 22 36860804 intron variant G/A snv 0.39 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs3890745
MMEL1
0.925 0.200 1 2622185 intron variant T/C snv 0.40 4
rs751837
CDC42BPB
0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs1323292
LOC105371664
0.882 0.160 1 192571891 intron variant G/A snv 0.86 3
rs1444766
KALRN
0.882 0.160 3 124206424 intron variant A/G;T snv 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs9831894
CD86
0.882 0.120 3 122081640 intron variant A/C snv 0.31 3
rs13255292
PVT1
0.925 0.120 8 128064327 intron variant C/T snv 0.24 2
rs1880030
BCL7A
0.925 0.120 12 122046634 intron variant G/A snv 0.39 2
rs2681416
CD86
0.925 0.120 3 122098766 intron variant G/A snv 0.26 2
rs79464052
ARAP3
1.000 0.120 5 141655607 intron variant G/C snv 7.1E-02 7.8E-02 1
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs7712513
LOC101927357
0.925 0.120 5 122582513 intergenic variant G/T snv 0.71 2
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 2
rs6773363 1.000 0.120 3 27752141 intergenic variant T/A;C snv 1
rs7765004 0.925 0.120 6 113750518 regulatory region variant A/C snv 0.32 2