Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1059611
LPL
8 19967052 3 prime UTR variant T/C snv 0.13 3
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 4
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15 2
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15 1
rs11644601
RRN3 ; PDXDC1
16 15078261 intron variant T/C snv 0.21 4
rs17267292
GPC5 ; LOC105370315
13 92670893 intron variant T/C snv 0.22 2
rs11075253
PDXDC1 ; NTAN1
16 15054789 intron variant C/A snv 0.22 1
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs331
LPL
8 19962894 intron variant G/A snv 0.30 4
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38 1
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs7228085
LOC105372112
18 49634444 intergenic variant A/G snv 0.53 1
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs1168041
DOCK7
1 62494579 non coding transcript exon variant T/C snv 0.61 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81