Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10489744 0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs10503253 0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs11756438 0.925 0.040 6 118672469 intron variant C/A snv 0.42 3
rs11789399 0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12325410 0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs12661338 0.925 0.040 6 118473527 intron variant C/A snv 0.35 2
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs12966547 0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs13061878 0.925 0.040 3 61634560 intron variant A/T snv 9.7E-02 2
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs1334489 0.925 0.040 6 118318224 downstream gene variant T/A snv 0.37 2
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1412005 0.925 0.040 9 90646879 upstream gene variant T/A;G snv 3