Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3745442
LAIR1
19 54361091 missense variant G/C snv 0.99 1
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs830948
LRP2
2 169358254 intron variant G/A snv 0.99 3
rs556766
PIGO
9 35089051 3 prime UTR variant A/C snv 1.00 0.98 1
rs2321168
STARD13 ; STARD13-AS
13 33279354 non coding transcript exon variant G/A snv 0.98 4
rs891142
CETP
16 56970065 intron variant T/C snv 0.97 1
rs567279
PDE4B
1 66222346 intron variant G/T snv 0.97 4
rs891141
CETP
16 56969811 intron variant G/T snv 0.96 1
rs231774
CTLA4
2 203867500 upstream gene variant T/A snv 0.96 1
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs8056298
ABCC1
16 16142666 3 prime UTR variant T/G snv 0.95 1
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs4402881
GLB1
3 33012839 intron variant T/C snv 0.93 2
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 2
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 3
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 1
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 3
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