Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 22
rs2738783 0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs7656411 0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs3024971 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs7192 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs1555549674 0.882 0.240 17 42223402 missense variant T/G snv 6
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1701704 0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs4512342 0.827 0.120 8 32750356 intron variant T/G snv 0.12 5
rs9372120 0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs2073440
HDC
0.851 0.200 15 50242317 missense variant T/G snv 3.4E-02 5.9E-02 4
rs3134792 0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs993226 0.851 0.160 12 84492794 intergenic variant T/G snv 6.3E-02 4
rs10056340 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 3
rs1655558 0.925 0.080 15 41495387 intron variant T/G snv 0.66 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs301805 1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs369252 0.882 0.400 1 228344451 intron variant T/G snv 0.74 3