Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 4
rs327
LPL
8 19962025 intron variant T/G snv 0.31 4
rs4698036 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 4
rs10513621 3 166009331 intergenic variant T/G snv 9.1E-02 1
rs11694728
ICA1L
2 202801596 intron variant T/G snv 0.39 1
rs11711013 3 165719779 intron variant T/G snv 0.32 1
rs12107166
BCHE
3 165779505 intron variant T/G snv 0.13 1
rs12490216 3 165933412 intergenic variant T/G snv 9.9E-02 1
rs12493215 3 165987906 intergenic variant T/G snv 0.22 1
rs1355535
BCHE
3 165787971 intron variant T/G snv 0.58 1
rs16839922 2 203575622 intergenic variant T/G snv 0.31 1
rs1707709 3 165721745 intron variant T/G snv 0.18 1
rs17659116 3 165892711 intergenic variant T/G snv 8.1E-02 1
rs282185 3 165897071 intergenic variant T/G snv 0.50 1
rs282195 3 165926523 intergenic variant T/G snv 0.56 1
rs3845802
WDR12
2 202875949 3 prime UTR variant T/G snv 0.42 1
rs6445180 3 166042918 intergenic variant T/G snv 0.58 1
rs6751448
NBEAL1
2 203141914 intron variant T/G snv 0.47 1
rs6785268
LOC105374191
3 164495329 intergenic variant T/G snv 0.29 1
rs6801661 3 166121774 intergenic variant T/G snv 0.21 1
rs7349596 3 165680167 intron variant T/G snv 0.10 1
rs9848129 3 165727298 intron variant T/G snv 7.9E-02 1
rs9873779
BCHE
3 165790314 intron variant T/G snv 0.65 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25