Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10100085 8 40198735 regulatory region variant C/A;G snv 1
rs10109417
DPYSL2
8 26530784 intron variant C/A;T snv 1
rs1011416
LINC00693 ; RBMS3
3 28755186 intron variant T/C snv 0.15 1
rs10120219
LOC105376158
9 95602265 intron variant C/A;T snv 1
rs10121511 9 96626342 intergenic variant A/C;T snv 1
rs10121673 9 108469029 regulatory region variant C/T snv 0.32 1
rs10128898
ERC1
12 1385266 intron variant G/A;T snv 1
rs10129429 14 91964487 downstream gene variant G/A;C snv 1
rs10131337
PAX9
14 36675311 intron variant C/T snv 0.19 1
rs1013209 8 24258791 intergenic variant C/T snv 0.28 2
rs10132476
CCDC197
14 94001945 intron variant G/T snv 0.39 1
rs10146757 14 95073400 intergenic variant A/G;T snv 1
rs10150698
LOC105370679 ; ANKRD9
14 102511539 upstream gene variant T/C snv 0.48 1
rs10152591
DRAIC ; LOC107984788
15 69755818 intron variant A/C snv 9.8E-02 2
rs10155941 7 134737981 upstream gene variant T/C snv 0.43 1
rs10157941
PODN
1 53083314 intron variant C/G snv 0.25 1
rs10165255
CYS1
2 10059474 intron variant A/G snv 0.59 2
rs10179158 2 65784898 intron variant T/C;G snv 1
rs10185143 2 24927889 intergenic variant T/C;G snv 0.57 1
rs10185917 2 171508843 intergenic variant A/G;T snv 1
rs10187066
ZNF142
2 218650036 intron variant A/G snv 0.45 2
rs10188078 2 113694652 intron variant G/A snv 0.15 1
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs10192454
GLI2
2 120865193 intron variant G/C snv 0.60 1
rs10198628 2 12824371 intron variant A/G snv 0.59 2