Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs11563251 2 233770738 3 prime UTR variant C/T snv 0.19 5
rs11891311 2 233730664 intron variant G/A snv 0.42 4
rs6741669 2 233744546 intron variant A/G snv 0.55 3
rs4148324 2 233764076 intron variant T/A;G snv 0.36 3
rs6715325 2 233726595 intron variant T/C snv 0.46 3
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 3
rs6714634 2 233756119 non coding transcript exon variant T/C snv 0.30 3
rs10179091 2 233749337 intron variant T/C snv 0.49 3
rs28900396 2 233761914 intron variant T/C snv 6.4E-02 3
rs10178992 2 233749231 intron variant T/A snv 0.37 3
rs4124874 0.851 0.120 2 233757013 intron variant T/A;G snv 3
rs6431628 2 233738832 intron variant A/G snv 0.56 3
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs4148326 0.925 0.080 2 233764816 intron variant T/C snv 0.49 3
rs7574296 2 233729603 synonymous variant A/G snv 0.49 0.54 3
rs7597496 2 233721797 non coding transcript exon variant A/C;G snv 3
rs17862875 2 233740656 intron variant G/A snv 0.30 3
rs10929301 2 233755003 splice region variant C/G;T snv 0.48 3
rs3806596 2 233729061 intron variant T/C snv 0.56 3
rs4663971 2 233765606 intron variant C/G;T snv 0.50 3
rs4399719 2 233757815 intron variant T/G snv 0.56 3
rs7564935 2 233736540 intron variant G/T snv 0.37 3
rs1983023 2 233728376 intron variant T/C snv 0.46 3