Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs752596535
LDLR
0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs755001634
FOLH1
0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 11
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs137852912
PCSK9
0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs3732581
PARL
0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs6850
LOC105375259 ; PPIA
0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9