Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 3
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 2
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
rs67418890 1 161571067 intron variant T/A;C snv 1
rs72669744 1 55650832 intron variant C/T snv 2.8E-02 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 5
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 4
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 3
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 3
rs506585 2 21174310 intergenic variant G/A;C;T snv 3
rs312985 2 21155933 regulatory region variant A/G snv 0.75 1
rs115136538
ADAMTS3
4 72456848 intron variant T/C snv 5.7E-03 1
rs6917603
ZNRD1ASP
6 30049294 intron variant T/C snv 0.15 1
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15 1
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs331
LPL
8 19962894 intron variant G/A snv 0.30 3
rs1059611
LPL
8 19967052 3 prime UTR variant T/C snv 0.13 1
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 1