Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 4
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3