Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575934
IL12RB1
0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 4
rs3800229
FOXO3
1.000 0.040 6 108675760 intron variant G/T snv 0.54 4
rs11031731 0.925 0.040 11 32343884 upstream gene variant G/A snv 0.18 3
rs1131454
OAS1
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs2243268
IL4
0.882 0.040 5 132678271 intron variant A/C snv 0.23 3
rs5743604
TLR1
0.925 0.040 4 38799664 intron variant A/G snv 0.36 3
rs76600635
TLR1
0.925 0.040 4 38798702 missense variant A/G snv 8.2E-03 2.8E-03 3
rs10500804
CYP2R1
0.925 0.040 11 14888727 intron variant T/G snv 0.35 2
rs1055229
LINC01857
1.000 0.040 2 207666959 non coding transcript exon variant C/T snv 0.26 2
rs11466617
TLR10
1.000 0.040 4 38778850 intron variant T/C snv 0.13 2
rs11575935
IL12RB1
0.925 0.040 19 18063921 missense variant C/T snv 1.1E-02 5.7E-03 2
rs12939622
DDX52
1.000 0.040 17 37611503 3 prime UTR variant G/A snv 0.42 2
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs1650232
SFTPA2
1.000 0.040 10 79559511 splice region variant C/A;T snv 3.6E-03; 0.71 2
rs17722851
NOS2
0.925 0.040 17 27783810 intron variant T/A snv 9.9E-02 2
rs1974675
IL18R1
1.000 0.040 2 102369915 intron variant G/A snv 0.45 2
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs2280788
CCL5 ; LOC105371744
0.925 0.040 17 35880401 5 prime UTR variant G/C snv 2.0E-02 2
rs2723187
IL37
1.000 0.040 2 112917692 missense variant C/T snv 6.8E-02 1.0E-01 2
rs35037722 0.925 0.040 17 78355453 upstream gene variant G/A;C snv 2
rs3731863
SLC11A1
0.925 0.040 2 218387485 intron variant C/T snv 8.0E-02 2
rs375947
IL12RB1
1.000 0.040 19 18069641 missense variant A/G snv 0.29 0.29 2
rs401502
IL12RB1
0.925 0.040 19 18069603 missense variant C/A;G;T snv 0.28; 3.2E-05 2
rs4262994
SYNRG
1.000 0.040 17 37591398 intron variant A/C snv 0.17 2
rs4921437
UBLCP1
0.925 0.040 5 159263943 intron variant T/A;C snv 2