Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs9358901 0.925 0.120 6 26024208 downstream gene variant G/T snv 0.67 5
rs1540275 0.925 0.120 6 26036248 upstream gene variant T/A;C snv 4
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 4
rs2051541 0.925 0.120 6 25944983 regulatory region variant A/G snv 0.47 4
rs4698036 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 4
rs6834555 0.882 0.200 4 10060702 regulatory region variant G/A snv 0.74 4
rs714873 0.882 0.200 4 10057994 upstream gene variant G/A snv 0.74 4
rs807214 0.925 0.120 6 26061541 intergenic variant G/A;C snv 4
rs9291683 0.925 0.120 4 10322536 intergenic variant G/A;C;T snv 4
rs9295678 0.925 0.120 6 25936805 intergenic variant G/A snv 0.45 4
rs9379801 0.925 0.120 6 25901483 intergenic variant T/C snv 0.48 4