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
rs10415893 1.000 19 17401603 upstream gene variant G/A snv 0.18 1
rs1047552
APH1B
0.925 0.080 15 63305658 missense variant T/A;G snv 6.1E-02 4.7E-02 2
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs1063320
HLA-G
0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10808739
CYP7B1
0.882 8 64727703 intron variant G/A snv 0.24 6
rs10831234
ANKRD49 ; MRE11
1.000 11 94500021 downstream gene variant C/T snv 0.11 1
rs10892324
SLC37A4
0.925 11 119032329 upstream gene variant T/A;G snv 5
rs11038628
TRIM5
1.000 11 5667710 missense variant C/T snv 0.14 0.14 1
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs11212495
CUL5
1.000 11 108048172 intron variant A/G;T snv 1
rs11231017 0.925 11 62293877 downstream gene variant G/A snv 0.29 5
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11649112
LOC107984137 ; SHISA9
0.925 16 13267554 intron variant G/A snv 0.22 5
rs11790131
LOC105375988
0.882 0.080 9 19469848 intergenic variant G/A;T snv 6
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs12460243
FBN3
0.925 19 8066356 intron variant G/A snv 0.14 5
rs1291142
SAMHD1
1.000 20 36896959 intron variant A/G;T snv 1
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs139292
APOBEC3H
1.000 22 39100318 inframe deletion CAA/- delins 1
rs139297
APOBEC3H
1.000 22 39101399 missense variant G/A;C;T snv 4.0E-06; 0.47 1