Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs55951658
CYP3A4
0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs5925
LDLR
0.851 0.200 19 11120205 synonymous variant T/C snv 0.42 0.37 7
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs529038
ROS1
0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 6
rs619203
ROS1
0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 6
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5
rs1057335
SERPINF2
0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs699473
SOD3
0.827 0.160 4 24795181 intron variant C/T snv 0.54 5
rs12342
ADIPOR2
0.851 0.240 12 1787714 3 prime UTR variant C/A;T snv 4
rs4073259
ALOX5AP
0.882 0.160 13 30732134 intron variant G/A snv 0.49 4
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4