Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs3917779
SELP
0.925 0.280 1 169601610 intron variant G/A snv 0.22 2
rs4865047
CEP135
0.925 0.240 4 55955640 intron variant C/T snv 0.12 2
rs1000708
SLC16A7
1.000 0.160 12 59689707 intron variant C/T snv 0.58 1
rs1144964
CPM
1.000 0.160 12 68944857 intron variant G/C;T snv 1
rs11488711
LINC02815 ; LINC02814
1.000 0.160 1 229105486 intron variant C/T snv 0.15 1
rs114921230
STUM
1.000 0.160 1 226595161 intron variant G/A snv 3.6E-02 1
rs116396065 1.000 0.160 8 121117030 intron variant T/A snv 8.4E-02 1
rs3081219
WDR72
1.000 0.160 15 53583969 intron variant GAGA/-;GA delins 1
rs4726066
PRKAG2
1.000 0.160 7 151625186 intron variant G/A;C snv 1
rs61811867
KCNN3
1.000 0.160 1 154802768 intron variant C/T snv 0.13 1
rs71354195
ZFP82
1.000 0.160 19 36385416 intron variant G/C snv 5.3E-02 1
rs72740408 1.000 0.160 1 191136701 intron variant G/A snv 0.17 1
rs73050171
NAALADL2
1.000 0.160 3 174801688 intron variant G/A snv 0.11 1
rs73228199
CD96
1.000 0.160 3 111597517 intron variant G/A snv 0.11 1
rs74705672
OC90
1.000 0.160 8 132042380 intron variant A/T snv 4.9E-02 1
rs7533141
GPATCH2
1.000 0.160 1 217543535 intron variant T/C snv 0.57 1
rs7604016
COMMD1
1.000 0.160 2 61965000 intron variant T/A;C snv 1
rs78464534
DPP10
1.000 0.160 2 115234275 intron variant C/A;G snv 1
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs184340784 0.925 0.160 1 4529823 intergenic variant C/T snv 6.1E-04 2
rs1902491 0.925 0.240 4 155134181 intergenic variant C/A;T snv 2
rs200295620 0.925 0.160 3 168172398 intergenic variant T/-;TT delins 5.7E-03 2
rs11201335 1.000 0.160 10 85018443 intergenic variant C/G;T snv 1