Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs1034589
RNF185
1.000 0.120 22 31183247 intron variant C/T snv 0.79 1
rs16996381 1.000 0.120 22 36115231 intergenic variant G/A snv 0.31 1
rs17809399
LARGE1
1.000 0.120 22 33861145 intron variant G/A snv 0.21 1
rs4820043
LIMK2
1.000 0.120 22 31251108 intron variant A/G;T snv 1
rs5749286
SFI1 ; DRG1
1.000 0.120 22 31504373 intron variant C/A;T snv 1
rs5749682
LARGE1
1.000 0.120 22 33852326 intron variant C/A snv 0.17 1
rs5750250
MYH9
1.000 0.120 22 36312438 intron variant G/A;T snv 1
rs735853
MYH9
1.000 0.120 22 36283169 intron variant C/G snv 0.34 1
rs2234694
SOD1
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs12976445
SPACA6 ; SPACA6P-AS ; MIRLET7E ; MIR125A
0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7