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
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs4565946 0.827 0.080 12 71942989 intron variant C/A;G;T snv 7