Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs7209436 0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs10835210 0.882 0.040 11 27674363 intron variant C/A;G snv 4