Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 3
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 5
rs622082
IGHMBP2
0.925 0.080 11 68936491 missense variant A/G snv 0.29 0.25 1
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs10838686
MADD
11 47289816 intron variant G/C;T snv 4.2E-06; 0.26 1
rs2279238
NR1H3
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26 1
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 1
rs2229357
INHBC
12 57449928 missense variant G/A snv 0.22 0.19 2
rs79949326
DAGLB
7 6421679 intron variant C/G;T snv 2.9E-05; 0.21 1
rs2074158
DHX58
1.000 0.040 17 42105145 missense variant T/C snv 0.21 0.33 2
rs28932178
NSD1
5 177210575 missense variant T/C snv 0.20 0.16 1
rs2853579
ABCA1
9 104828991 synonymous variant G/T snv 0.20 0.23 3
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs12225230
SIK3
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06 3
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 4
rs17513135
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570014 intron variant C/A;T snv 0.17 0.16 2
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 1
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 1
rs3785100
SLC12A4
16 67964017 missense variant T/C snv 0.15 0.16 1
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 3
rs267738
CERS2
1.000 0.040 1 150968149 missense variant T/A;G snv 4.0E-06; 0.15 4
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs17688076
PLA2G15
16 68252524 intron variant C/A snv 0.14 0.11 2
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26