Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7117111
CUL5
1.000 11 108046360 synonymous variant A/G snv 0.68 0.59 1
rs139297
APOBEC3H
1.000 22 39101399 missense variant G/A;C;T snv 4.0E-06; 0.47 1
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs1799937
WT1
0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 3
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs6850
LOC105375259 ; PPIA
0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9
rs2229116
RYR3
0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11038628
TRIM5
1.000 11 5667710 missense variant C/T snv 0.14 0.14 1
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs6508
WT1-AS
0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16 3
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1047552
APH1B
0.925 0.080 15 63305658 missense variant T/A;G snv 6.1E-02 4.7E-02 2
rs8177832
APOBEC3G
0.851 0.160 22 39081561 missense variant A/G snv 5.9E-02 0.14 5
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs35467001
SDK2
0.882 0.080 17 73383923 missense variant G/A snv 5.3E-02 6.3E-02 6
rs1800451
MBL2
0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs183662584
CCR5 ; CCR5AS
1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2
rs541069027
CCR5 ; CCR5AS
1.000 3 46373290 missense variant G/A snv 1.8E-04 4.2E-05 1
rs146215995
TRIM5
1.000 11 5679850 missense variant C/A;T snv 8.0E-06; 9.5E-05 1