Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10155981 7 22716844 intron variant C/T snv 0.21 2
rs10164928 2 233893139 regulatory region variant C/T snv 5.8E-02 2
rs10167119 2 233680666 intron variant T/C snv 0.34 3
rs10168155 2 233688190 intron variant C/T snv 0.39 3
rs10168333 2 233688342 intron variant C/T snv 0.39 3
rs10170160 2 233791932 intron variant T/C snv 0.42 2
rs10171367 2 233689021 intron variant C/A;G snv 3
rs10175809 2 233688219 intron variant T/A snv 0.39 3
rs10175828 2 233473171 downstream gene variant G/C;T snv 2
rs10175949 2 233804275 intron variant G/A snv 0.89 2
rs10176426 2 233671269 intron variant C/T snv 7.1E-02 2
rs10178992 2 233749231 intron variant T/A snv 0.37 3
rs10179091 2 233749337 intron variant T/C snv 0.49 3
rs10179094 2 233689179 intron variant T/A snv 0.34 3
rs10189426 2 233674844 intron variant C/T snv 8.2E-02 2
rs10197460 2 233680544 intron variant G/T snv 0.34 3
rs10199293 2 233680858 intron variant T/C snv 0.65 2
rs10199882 2 233776618 intron variant T/C snv 0.15 2
rs10203853 1.000 0.080 2 233778772 intron variant A/G;T snv 2
rs10207194 2 233791739 intron variant C/A snv 0.40 2
rs10209214 2 233778937 intron variant T/C snv 0.26 2
rs10210058 2 233616709 upstream gene variant C/T snv 0.23 2
rs1042590 2 233618139 synonymous variant G/A snv 2.8E-04 9.1E-04 2
rs1042597 2 233618225 missense variant C/G;T snv 0.27; 4.0E-06 2
rs1042640 1.000 0.080 2 233772898 3 prime UTR variant G/A;C;T snv 2