Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs7867155 0.925 0.080 9 96065532 intron variant C/T snv 0.13 2