Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs2072136 0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs1732778 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 5
rs2285932 0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5
rs1131454 0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs179010 0.882 0.200 X 12884766 intron variant T/C snv 3
rs1382022101 1.000 0.040 9 99828794 missense variant C/T snv 1
rs5741880 1.000 0.040 X 12869297 intron variant G/T snv 0.20 1