Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10502995 18 55138645 regulatory region variant G/A snv 0.20 1
rs11972901 7 85966605 intergenic variant A/G snv 0.47 1
rs1453029 18 41000207 intergenic variant T/C snv 7.0E-02 1
rs1737076 6 29757544 intron variant A/G snv 0.45 1
rs17450420 13 104386796 intergenic variant A/G snv 5.9E-02 1
rs2378002 1 218749016 intergenic variant G/T snv 5.9E-02 1
rs2984526 9 72372344 intergenic variant C/G snv 0.48 1
rs4283388 2 172374994 downstream gene variant C/T snv 0.33 1
rs4503732 15 46350065 intron variant C/A;G;T snv 0.92 1
rs6023640 20 54842266 intergenic variant T/G snv 0.73 1
rs7206735 16 50114597 intron variant T/C snv 0.39 1
rs753544 6 29812752 upstream gene variant C/T snv 0.27 1
rs896570 10 47145727 intergenic variant C/T snv 0.50 1
rs902907 9 79199649 upstream gene variant G/A snv 0.56 1
rs9288520 2 216616548 intergenic variant G/A snv 0.14 1
rs4148641
ABCC8
11 17399926 intron variant G/A;T snv 1
rs2803270
AGBL4
1 48565566 intron variant C/T snv 0.61 1
rs4908343
AHDC1
1 27605187 upstream gene variant G/A snv 0.61 1
rs581037
AHR
7 17050319 intron variant C/T snv 0.26 1
rs3807390
AMPH
7 38533831 intron variant T/C snv 0.30 1
rs11776675
CDH17
8 94163787 intron variant T/C snv 0.23 1
rs747621669
CDKN2A
9 21970988 missense variant C/T snv 4.1E-06 1
rs11254327
CUBN
10 17006709 intron variant C/T snv 0.40 1
rs9566910
DGKH
13 42076866 intron variant G/A snv 0.36 1
rs2409764
FAM167A ; FAM167A-AS1
8 11423764 3 prime UTR variant A/G;T snv 1