Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs104893636
HOXD4 ; HOXD3
0.882 0.120 2 176151875 missense variant A/C;T snv 5.2E-06; 7.9E-04 3
rs78380171
LOC101927518
0.925 0.120 3 86720838 intergenic variant A/G snv 6.6E-03 2
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs11099592
HPSE
0.851 0.160 4 83309466 missense variant T/C snv 0.78 0.80 5
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs6535455
HPSE
0.851 0.160 4 83310951 intron variant T/A;C snv 4
rs10519612
IL15
0.882 0.120 4 141732548 intron variant A/C snv 0.10 3
rs76996680
LEF1
0.882 0.120 4 108163665 missense variant G/A snv 1.0E-03 3.4E-04 3
rs772470710
NSD2
0.882 0.120 4 1961074 missense variant G/A snv 4.0E-06 3
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs3733890
BHMT ; DMGDH
0.708 0.480 5 79126136 missense variant G/A snv 0.30 0.28 16
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs1194008138
NR3C1
0.882 0.120 5 143400121 missense variant T/C snv 4.0E-06 3