Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs12526453
PHACTR1
0.827 0.160 6 12927312 intron variant C/G snv 0.27 5
rs2048327
SLC22A3
0.851 0.120 6 160442500 intron variant T/C snv 0.28 5
rs1240681880
DNAH8
0.882 0.160 6 38722870 missense variant G/A snv 2.1E-05 3
rs374691452
DNAH8
0.925 0.120 6 38723443 missense variant T/A;C snv 4.2E-06; 2.5E-05 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs751141
EPHX2
0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs118204060
LPL
0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 9
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs121909374
MYBPC3
0.790 0.120 11 47342578 stop gained C/A;G snv 1.3E-05 7
rs33972927
HBB
0.925 0.080 11 5226612 missense variant A/G snv 2
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs2228576
SCNN1A ; LOC107984500
0.851 0.160 12 6347896 missense variant T/A;C;G snv 4.5E-06; 0.69 4
rs104894503
TPM1
0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs746394586
TPM1
1.000 0.080 15 63057022 missense variant A/G snv 1
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58