Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
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