Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs3957357
GSTA1
0.807 0.280 6 52803889 upstream gene variant A/G snv 0.63 7
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs1800683
LOC100287329 ; LTA
0.807 0.240 6 31572294 5 prime UTR variant G/A;C snv 0.39 6
rs2844484
LTA ; LOC100287329
0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6
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
rs116446171 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 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
rs1178732315
GBA
0.882 0.240 1 155236381 missense variant A/G snv 1.4E-05 3
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
rs1239470707
PPARG
0.925 0.120 3 12416785 missense variant C/A snv 2