Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2652106
VCAN
1.000 0.040 5 83498217 intron variant G/T snv 0.39 1
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs3781590
LRP5
1.000 0.040 11 68391684 intron variant G/A snv 0.35 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs12695895
AGTR1
0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1385526
LRP1
1.000 0.040 12 57138966 intron variant G/C snv 0.26 1
rs7579
CCDC152 ; SELENOP
0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs8003379
MTHFD1
0.882 0.160 14 64406881 intron variant A/C snv 0.23 3
rs9316871 1.000 0.040 13 22287782 intergenic variant A/G snv 0.22 1
rs326118
MTRR ; FASTKD3
0.925 0.080 5 7868430 intron variant T/G snv 0.21 2
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1057335
SERPINF2
0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs6674171
TDRD10
1.000 0.040 1 154519207 intron variant A/G;T snv 0.19 1
rs10985349
DAB2IP
1.000 0.040 9 121662964 intron variant C/T snv 0.17 1
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs58749629
PCIF1
1.000 0.040 20 45942678 intron variant G/A;T snv 0.13 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15