Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 6
rs247616 1.000 0.040 16 56955678 intergenic variant C/T 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
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 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
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 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
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 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
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5