Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1182188 0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs798502 1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs798489 7 2762169 splice donor variant C/T snv 0.20 3
rs798491 7 2760887 intron variant A/C;G snv 2
rs71026567 7 2831405 intron variant TTTTTTTTTTT/-;T;TT;TTTT;TTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT delins 2
rs798497 7 2756323 intron variant A/G snv 0.25 1
rs33932857 7 2736084 intron variant G/A snv 0.29 1
rs2266925 7 2823257 intron variant C/T snv 0.25 1
rs13226653 7 2786022 intron variant G/A;T snv 1
rs201517448 7 2842084 intron variant AGGAAGGAA/-;AGGAAGGAAAGGAAGGAA;AGGAAGGAAAGGAAGGAAAGGAAGGAAAGGAAGGAA delins 9.9E-03 1
rs3831679 7 2830954 intron variant AAAA/-;AA;AAA;AAAAA delins 1
rs771273709 7 2812656 intron variant C/A snv 1
rs1182180 7 2833645 intron variant G/A;T snv 0.42 1
rs7777484 7 2774637 intron variant A/G snv 0.38 1
rs35957220 7 2772998 intron variant C/A;G snv 1
rs798528 7 2732797 intron variant A/C snv 0.25 1