Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs183662584
CCR5 ; CCR5AS
1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2
rs4704846
HAVCR2
1.000 5 157086333 3 prime UTR variant G/A snv 0.79 2
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2
rs753269867
THBS1
0.925 0.080 15 39582202 missense variant G/C snv 6.3E-05 2
rs2234591
WT1
0.925 0.080 11 32399873 intron variant T/C snv 1.4E-03 2
rs1799937
WT1
0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 3
rs6508
WT1-AS
0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16 3
rs2301254
WT1-AS ; WT1
0.882 0.160 11 32436129 intron variant A/G snv 0.48 3
rs766662990
LOC105371744 ; CCL5
0.851 0.120 17 35878529 missense variant C/T snv 1.6E-05 7.0E-06 4
rs11231017 0.925 11 62293877 downstream gene variant G/A snv 0.29 5
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5
rs17151904 0.925 7 25568789 TF binding site variant G/A;C snv 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
rs8177832
APOBEC3G
0.851 0.160 22 39081561 missense variant A/G snv 5.9E-02 0.14 5
rs17038463
CNTN6
0.925 3 1383484 intron variant T/C;G snv 5
rs12460243
FBN3
0.925 19 8066356 intron variant G/A snv 0.14 5
rs17691394
GRM8
0.925 7 126684537 intron variant A/G snv 0.13 5
rs17169
LINC00298 ; LINC00299
0.925 2 8037334 intron variant G/T snv 0.13 5
rs7576600
LOC105374497
0.925 2 40840846 intergenic variant C/A;G snv 5
rs11649112
LOC107984137 ; SHISA9
0.925 16 13267554 intron variant G/A snv 0.22 5
rs608114
LOC107986626
0.925 6 95928822 intron variant A/T snv 0.95 5
rs30388
MAF
0.925 16 79580219 regulatory region variant T/C;G snv 5