Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs573775
ATG5
0.851 0.320 6 106316991 intron variant G/A snv 0.34 4
rs199422295
TERT
0.882 0.120 5 1279376 missense variant C/T snv 3
rs11465797
IL23R ; C1orf141
1.000 0.040 1 67200769 missense variant C/A snv 2
rs803360
ATG5
1.000 0.040 6 106318254 intron variant G/A;C snv 1
rs2317130
TGFB1 ; B9D2
1.000 0.040 19 41355769 intron variant C/G;T snv 1