Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042489 0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25490 0.851 0.120 19 43552189 missense variant T/C snv 7.2E-03 2.6E-02 4
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs3798577 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs864745 0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs2077647 0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16