Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs143633948
ARG1
0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs73132848
CAV3 ; OXTR
0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs10808739
CYP7B1
0.882 8 64727703 intron variant G/A snv 0.24 6
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 6
rs35897606
KIAA1549L
0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs79709413
LOC105370118
0.882 0.080 13 24740488 upstream gene variant G/T snv 4.7E-02 6
rs73084982
LOC105372508
0.882 0.080 20 3430406 intergenic variant G/A snv 3.5E-02 6
rs11790131
LOC105375988
0.882 0.080 9 19469848 intergenic variant G/A;T snv 6
rs35467001
SDK2
0.882 0.080 17 73383923 missense variant G/A snv 5.3E-02 6.3E-02 6
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