Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs643531
TTC39B
9 15296036 intron variant C/A snv 0.89 2
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 3
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 2
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 1
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87 3
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs7240405
LOC105372112
18 49632720 intergenic variant A/G snv 0.86 2
rs1540037
LOC105372112
18 49656294 TF binding site variant A/G snv 0.83 3
rs261338
LIPC ; LIPC-AS1 ; ALDH1A2
15 58442806 intron variant A/G snv 0.83 5
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 3
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs261336
ALDH1A2 ; LIPC ; LIPC-AS1
15 58450219 intron variant G/A snv 0.81 5
rs289742
CETP
16 56983850 downstream gene variant C/G snv 0.80 2
rs2980885 8 125462064 upstream gene variant G/A snv 0.80 1
rs4783962
CETP
16 56961126 upstream gene variant T/C snv 0.80 2
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs4587963
CETP
16 56963457 intron variant A/T snv 0.79 2
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs158480
CETP
16 56974315 intron variant G/A snv 0.78 2
rs2954033 8 125481504 intron variant A/G snv 0.76 4
rs2954026 8 125472284 intron variant T/G snv 0.76 1
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 3