Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs11644601
RRN3 ; PDXDC1
16 15078261 intron variant T/C snv 0.21 4
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 4
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 4
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 4
rs331
LPL
8 19962894 intron variant G/A snv 0.30 4
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs1059611
LPL
8 19967052 3 prime UTR variant T/C snv 0.13 3
rs1168041
DOCK7
1 62494579 non coding transcript exon variant T/C snv 0.61 2
rs17267292
GPC5 ; LOC105370315
13 92670893 intron variant T/C snv 0.22 2
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02 2
rs312985 2 21155933 regulatory region variant A/G snv 0.75 2
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15 2
rs11075253
PDXDC1 ; NTAN1
16 15054789 intron variant C/A snv 0.22 1
rs115136538
ADAMTS3
4 72456848 intron variant T/C snv 5.7E-03 1
rs1168029
DOCK7
1 62503731 intron variant G/A;C snv 1
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15 1
rs17610395
CPT1A
11 68794860 missense variant C/G;T snv 1
rs181807530
MINK1
17 4871519 intron variant C/G snv 4.8E-03 1