Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11200014 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs2981575 0.882 0.120 10 121586602 intron variant G/A snv 0.54 3
rs2981579 0.776 0.280 10 121577821 intron variant A/G snv 0.53 2
rs3135718 0.882 0.160 10 121594355 intron variant C/T snv 0.54 2
rs3135724 1.000 0.080 10 121592706 intron variant C/G;T snv 2
rs10510097 1.000 0.080 10 121568362 intron variant C/T snv 0.19 1
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 1
rs2420946 0.851 0.160 10 121591810 intron variant T/C snv 0.56 1
rs2912774 0.925 0.080 10 121589148 intron variant T/A;G snv 1
rs2981578 0.925 0.080 10 121580797 intron variant C/A;T snv 1
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 1
rs35054928 0.851 0.080 10 121580918 intron variant C/- delins 1
rs3750817 0.851 0.080 10 121573063 intron variant C/G;T snv 1
rs45631563 1.000 0.080 10 121589810 intron variant A/T snv 3.6E-02 1