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
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12