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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs1200746244 0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs2239547 0.882 0.040 3 52821213 intron variant T/C snv 0.27 6