Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2239751
MAPKAPK3 ; CISH
0.882 0.120 3 50610457 5 prime UTR variant T/G snv 9.6E-02 7.1E-02 3
rs12331678
HPSE
0.925 0.120 4 83303254 intron variant T/G snv 0.82 2
rs3128917
HLA-DPA2
0.925 0.200 6 33092219 non coding transcript exon variant T/G snv 0.33 2
rs9277546
HLA-DPB1
0.925 0.200 6 33087569 3 prime UTR variant T/G snv 0.38 2
rs1126769
HLA-DPA1
1.000 0.080 6 33068658 missense variant T/G snv 0.24 0.29 1
rs2308911
HLA-DPA1
1.000 0.080 6 33069803 missense variant T/G snv 0.23 0.28 1
rs3130780
GTF2H4
1.000 0.080 6 30906531 upstream gene variant T/G snv 0.77 1
rs3756979
RN7SK ; GSTA4
1.000 0.080 6 52996406 upstream gene variant T/G snv 3.5E-03 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs2071353
HLA-DPA1 ; HLA-DPB1
1.000 0.080 6 33076480 intron variant T/C;G snv 1
rs6819823
IL15
1.000 0.080 4 141717598 5 prime UTR variant T/C;G snv 0.48 1
rs9380336
HLA-DPA1
1.000 0.080 6 33072959 intron variant T/C;G snv 0.28 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77