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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs28364997 0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs6782011 0.807 0.120 3 7457960 intron variant C/T snv 0.52 7