Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22