Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 3
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 3
rs331
LPL
8 19962894 intron variant G/A snv 0.30 3
rs506585 2 21174310 intergenic variant G/A;C;T snv 3
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 2
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 2
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02 2
rs1059611
LPL
8 19967052 3 prime UTR variant T/C snv 0.13 1
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
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 1
rs11644601
RRN3 ; PDXDC1
16 15078261 intron variant T/C snv 0.21 1
rs1168029
DOCK7
1 62503731 intron variant G/A;C snv 1
rs1168041
DOCK7
1 62494579 non coding transcript exon variant T/C snv 0.61 1
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15 1
rs17267292
GPC5 ; LOC105370315
13 92670893 intron variant T/C snv 0.22 1
rs312985 2 21155933 regulatory region variant A/G snv 0.75 1
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38 1
rs67418890 1 161571067 intron variant T/A;C snv 1
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15 1