Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs12913832 0.763 0.200 15 28120472 intron variant A/G snv 0.50 15