Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs7501939 0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs11651052 0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs11263763 0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs757210 0.807 0.160 17 37736525 intron variant C/G;T snv 6
rs2005705 0.925 0.120 17 37736310 intron variant G/A snv 0.46 2
rs3760511 0.925 0.080 17 37746322 upstream gene variant G/A;T snv 2
rs8064454 0.925 0.120 17 37741595 intron variant C/A;G snv 2
rs4794758 0.925 0.080 17 37720433 intron variant T/C snv 0.66 2
rs11649743 0.925 0.080 17 37714971 intron variant A/G snv 0.85 2