Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 3
rs28451064 0.925 0.080 21 34221526 intron variant G/A snv 9.2E-02 3
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 3
rs10131894 1.000 0.040 14 74980176 regulatory region variant C/G snv 0.49 2
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 2
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 2
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 2
rs28641753 0.925 0.160 3 104256574 intergenic variant C/T snv 4.5E-02 2
rs35237252 1.000 0.040 8 20012760 intergenic variant C/A;T snv 0.24 2
rs41269133 1.000 0.040 6 160666831 intron variant T/C snv 8.8E-02 2
rs4593108 0.925 0.080 4 147359849 regulatory region variant C/G snv 0.31 2
rs663640 1.000 0.040 18 60178844 intergenic variant C/T snv 0.23 2
rs7033354 1.000 0.040 9 16904848 intergenic variant C/T snv 0.62 2
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 2
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 2
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs10186133 1.000 0.040 2 113079367 downstream gene variant G/A;T snv 1
rs10221742 1.000 0.040 2 21196778 downstream gene variant G/A snv 0.32 1
rs10495907 1.000 0.040 2 43771587 upstream gene variant G/A snv 0.13 1
rs10793514 1.000 0.040 10 44001523 intergenic variant T/C snv 0.58 1
rs10951983 1.000 0.040 7 6406396 downstream gene variant A/G snv 0.15 1