Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6