Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs1562114190 0.790 0.160 6 78946061 frameshift variant A/- delins 21
rs1562134961 0.776 0.320 6 78969879 frameshift variant A/- delins 13
rs1085307845 0.752 0.320 6 79025582 missense variant G/T snv 21
rs1554210073 0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1555453538 0.807 0.280 15 89326678 frameshift variant A/- delins 7
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14