Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 6
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 5
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 5
rs74617384
LPA
0.925 0.080 6 160576086 intron variant A/G;T snv 5
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 5