Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs2073440
HDC
0.851 0.200 15 50242317 missense variant T/G snv 3.4E-02 5.9E-02 4
rs243864
MMP2
0.925 0.080 16 55478410 intron variant T/G snv 0.19 3
rs4822489
SPECC1L-ADORA2A ; ADORA2A ; ADORA2A-AS1
0.925 0.200 22 24437792 intron variant T/G snv 0.48 2
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs1805127
KCNE1
0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 6
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4
rs6026584
GNAS
0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs1429117513
LAG3
0.925 0.040 12 6775316 synonymous variant T/C snv 4.0E-06 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs13058338
RAC2
1.000 0.040 22 37236730 intron variant T/A;G snv 4
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs748379243
ERCC8
0.882 0.200 5 60928961 splice acceptor variant T/A;C snv 4.0E-06 7.0E-06 6
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4