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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs604300 1.000 0.080 3 127724009 intron variant A/G snv 0.91 3