Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs1179251 0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs992157 0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs60745952 0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs35301225 0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs3775292 0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5