Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs2070584
TIMP1 ; MIR4769 ; SYN1
0.790 0.200 X 47587120 intron variant T/G snv 0.44 8
rs12191786
CASC15
0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs12695895
AGTR1
0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs595244
FBN1
0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs8003379
MTHFD1
0.882 0.160 14 64406881 intron variant A/C snv 0.23 3
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs326118
MTRR ; FASTKD3
0.925 0.080 5 7868430 intron variant T/G snv 0.21 2
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs4988300
LRP5
0.925 0.120 11 68321363 intron variant G/T snv 0.50 2