Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 14
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 11
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188