Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10005067 4 87931491 intergenic variant T/A;C snv 1
rs10101385 8 118911611 regulatory region variant A/G snv 0.34 1
rs10120794 9 130550694 intergenic variant G/A snv 0.40 1
rs1037011 12 106909000 upstream gene variant T/C snv 0.64 1
rs10450586 11 27286936 intergenic variant G/C snv 0.60 1
rs10493013 1 22376542 regulatory region variant T/C snv 0.20 1
rs10735851 12 53349280 upstream gene variant G/A snv 0.68 1
rs10788264 10 122256471 downstream gene variant G/A;C snv 1
rs10872676 6 151622842 downstream gene variant C/A;T snv 1
rs11228240 11 68450822 downstream gene variant C/T snv 0.22 1
rs115242848 2 118750031 intergenic variant C/T snv 7.5E-03 1
rs11606709 11 46708972 downstream gene variant A/G snv 0.54 1
rs116926994 13 42503109 intergenic variant A/G snv 1.9E-02 1
rs11712608 3 143894341 intergenic variant C/A snv 0.23 1
rs11803476 1 22376832 regulatory region variant C/T snv 0.15 1
rs11810369 1 22361158 downstream gene variant G/A snv 0.22 1
rs11934731 4 87910097 intergenic variant G/A snv 0.67 1
rs11972702 7 38108059 regulatory region variant C/A;T snv 1
rs12197785 6 151639470 intergenic variant C/G;T snv 1
rs12561997 1 22375787 TF binding site variant G/A snv 0.15 1
rs12612325 2 118874676 intergenic variant G/A snv 0.26 1
rs12706298 7 120939583 intergenic variant C/A;G;T snv 1
rs12723796 1 22365113 non coding transcript exon variant G/A snv 0.16 1
rs12750721 1 22362780 downstream gene variant G/A snv 0.22 1
rs12756978 1 22358262 intergenic variant G/C snv 0.20 1