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
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 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
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4