Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16933829
PIK3C2A
0.925 11 17094129 intron variant T/C snv 6.2E-02 5
rs17038463
CNTN6
0.925 3 1383484 intron variant T/C;G snv 5
rs17151904 0.925 7 25568789 TF binding site variant G/A;C snv 5
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13 5
rs17691394
GRM8
0.925 7 126684537 intron variant A/G snv 0.13 5
rs30388
MAF
0.925 16 79580219 regulatory region variant T/C;G snv 5
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17 5
rs4835796
REEP2
0.925 5 138446426 3 prime UTR variant T/G snv 0.56 5
rs59440261
MICA
0.925 6 31403294 intron variant C/A snv 3.3E-02 5
rs608114
LOC107986626
0.925 6 95928822 intron variant A/T snv 0.95 5
rs61550741
TIAM1
0.925 21 31133966 intron variant A/G snv 0.12 5
rs6542826
SH3RF3 ; RANBP2
0.925 2 109433263 intron variant A/G snv 0.51 5
rs6594357 0.925 5 109205522 intergenic variant T/A;C snv 5
rs6723162 0.925 2 70875156 intergenic variant A/T snv 0.65 5
rs7458938 0.925 7 125820594 intergenic variant G/A snv 0.72 5
rs7576600
LOC105374497
0.925 2 40840846 intergenic variant C/A;G snv 5
rs2301254
WT1-AS ; WT1
0.882 0.160 11 32436129 intron variant A/G snv 0.48 3
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2
rs2234591
WT1
0.925 0.080 11 32399873 intron variant T/C snv 1.4E-03 2
rs4704846
HAVCR2
1.000 5 157086333 3 prime UTR variant G/A snv 0.79 2
rs10415893 1.000 19 17401603 upstream gene variant G/A snv 0.18 1
rs10831234
ANKRD49 ; MRE11
1.000 11 94500021 downstream gene variant C/T snv 0.11 1
rs11212495
CUL5
1.000 11 108048172 intron variant A/G;T snv 1
rs1291142
SAMHD1
1.000 20 36896959 intron variant A/G;T snv 1
rs139292
APOBEC3H
1.000 22 39100318 inframe deletion CAA/- delins 1