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
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
rs10175809 2 233688219 intron variant T/A snv 0.39 3
rs2741034 2 233640168 intron variant A/G snv 0.22 3
rs17864683 2 233670563 intron variant A/C;G snv 3
rs2741045 2 233671494 intron variant C/T snv 0.22 3
rs2741046 2 233671603 intron variant T/C snv 0.22 3
rs10168333 2 233688342 intron variant C/T snv 0.39 3
rs10197460 2 233680544 intron variant G/T snv 0.34 3
rs13002774 2 233685060 intron variant G/A;T snv 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
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
rs7608175 2 233690443 intron variant C/G snv 0.39 3