Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs754907741
HNF4A
1.000 0.040 20 44414567 missense variant G/A snv 1.2E-05 7.0E-06 2
rs779271027
HNF4A
1.000 0.040 20 44413723 missense variant A/C;G snv 4.0E-06; 8.0E-06 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs8111699
STK11
0.851 0.200 19 1209715 intron variant C/G snv 0.53 6
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs768925824
LDLR
0.925 0.040 19 11110693 missense variant G/A snv 4.0E-06 4
rs11672433
ANGPTL4
0.925 0.120 19 8373832 synonymous variant G/A;C snv 0.10; 4.0E-06 3
rs191885206
CYP4F12
1.000 0.080 19 15696024 missense variant T/C snv 7.0E-04 3.1E-04 3