Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs333 0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs10204525 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs3761549 0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs2239704 0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2233678 0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs13347 0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs2233406 0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26 12
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs1053004 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs12508721 0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs2233679 0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11