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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24