Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs871656 0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs3917265 1.000 0.120 2 102162001 intron variant T/C snv 0.50 2
rs13427957 1.000 0.080 2 102072571 intron variant C/T snv 0.46 1
rs4851541 2 102123999 intron variant G/T snv 0.40 1
rs150946191 2 102116028 intron variant T/G snv 1.9E-02 1
rs4141632 2 102140679 intron variant A/G;T snv 1
rs9284725 2 102128394 intron variant C/A;T snv 0.82 1
rs12712127 2 102110201 intron variant A/G snv 0.62 1
rs1558643 2 102115231 intron variant T/C;G snv 1
rs7588201 2 102129816 intron variant A/C snv 0.39 1
rs2228139 2 102165189 missense variant C/A;G snv 5.6E-02 1
rs3917254 2 102160058 intron variant G/A snv 0.16 1