Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28364997 0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs121909323 0.790 0.160 19 13277122 stop gained G/A snv 8
rs1555453538 0.807 0.280 15 89326678 frameshift variant A/- delins 7
rs1135402760 0.851 0.160 11 1451405 frameshift variant AG/- delins 6
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7794745 0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs1051312 0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs1460808228 0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4