Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19