Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14