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
rs6928977
AHI1
0.925 0.120 6 135305210 intron variant T/G snv 0.70 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs3138053
NFKBIA
0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 10
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs182123615
JAK2 ; INSL6
0.807 0.200 9 5070058 splice region variant T/C snv 3.6E-04 1.1E-03 7
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs9268403
TSBP1 ; TSBP1-AS1
0.807 0.240 6 32373696 intron variant T/C snv 0.24 6
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs644236
DROSHA
0.882 0.320 5 31409008 non coding transcript exon variant T/C snv 0.31 0.35 5
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs6763508
ULK4
0.851 0.160 3 41709497 intron variant T/C snv 0.30 4
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27 2
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50 1
rs3130237 1.000 0.120 6 33129784 downstream gene variant T/C snv 0.13 1