Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004638 1.000 0.040 9 22115590 intron variant A/C;T snv 3
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10965212 0.925 0.080 9 22023796 intron variant T/A;C;G snv 3
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs1537375 0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs445925 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs4977575 1.000 0.040 9 22124745 intron variant C/G;T snv 2
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs523096 0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs2026458 0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs496892 0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2891168 0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10738607 0.925 0.080 9 22088095 intron variant A/G snv 0.42 4