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
rs10519210 1.000 0.040 15 63445726 intergenic variant T/C;G snv 1
rs1520832 1.000 0.040 12 42859612 regulatory region variant T/C;G snv 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
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
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 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
rs11006544
LOC107984235
1.000 0.040 10 59510886 intergenic variant T/C snv 7.3E-03 3
rs11110004
ANKS1B
1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 3
rs148133894 1.000 0.040 16 24584678 intergenic variant T/C snv 2.4E-03 3
rs150381023
CELSR1
1.000 0.040 22 46423108 intron variant T/C snv 5.8E-03 3