Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11557467 0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs11078925 0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11557466 0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 3
rs11870965 0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12936231 0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs1054609 0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs4795397 0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 2
rs12150079 0.807 0.280 17 39869164 intron variant G/A snv 0.24 1