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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2710102 0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6