Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 4
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 3
rs10089517 0.925 0.040 8 59266162 intergenic variant C/A snv 0.31 2
rs10113215 1.000 0.040 8 59219635 intergenic variant A/G snv 0.33 1
rs10512441 1.000 0.040 17 32912627 regulatory region variant C/T snv 0.21 1
rs10936538 1.000 0.040 3 167439281 downstream gene variant C/A;T snv 1
rs11658305 1.000 0.040 17 7526004 intergenic variant A/C;T snv 1
rs1370156 1.000 0.040 15 34692682 intergenic variant G/C snv 0.67 1
rs1556867 1.000 0.040 1 164244449 intergenic variant C/T snv 0.24 1
rs1585471 1.000 0.040 4 111781479 regulatory region variant A/G snv 0.30 1
rs2218817 1.000 0.040 4 111689850 regulatory region variant G/A snv 0.32 1
rs61049169 1.000 0.040 2 146131140 intergenic variant G/A;C snv 1
rs6837348 1.000 0.040 4 111787647 intergenic variant G/A snv 0.28 1
rs73157695 1.000 0.040 21 45952033 intergenic variant G/A snv 0.29 1
rs9585327 1.000 0.040 13 100037100 intergenic variant G/A snv 0.36 1
rs864321670
ALDH18A1
0.763 0.320 10 95633012 missense variant C/T snv 24
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs7162310
APH1B
1.000 0.040 15 63279035 intron variant C/T snv 0.28 1
rs387907141
ARID1B
0.752 0.360 6 157181137 stop gained C/T snv 24
rs876657380
ARID1B
0.851 0.360 6 157181155 frameshift variant AA/- delins 11
rs4948523
BICC1
1.000 0.040 10 58579338 intron variant A/C snv 0.51 1
rs5022942
BMP3
1.000 0.040 4 81038812 intron variant A/G snv 0.59 1
rs1555639076
BPTF
0.790 0.400 17 67893677 splice donor variant A/- delins 16