Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs2229116
RYR3
0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs35897606
KIAA1549L
0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs17691394
GRM8
0.925 7 126684537 intron variant A/G snv 0.13 5
rs61550741
TIAM1
0.925 21 31133966 intron variant A/G snv 0.12 5
rs6542826
SH3RF3 ; RANBP2
0.925 2 109433263 intron variant A/G snv 0.51 5
rs8177832
APOBEC3G
0.851 0.160 22 39081561 missense variant A/G snv 5.9E-02 0.14 5
rs1799937
WT1
0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 3
rs2301254
WT1-AS ; WT1
0.882 0.160 11 32436129 intron variant A/G snv 0.48 3
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2
rs7117111
CUL5
1.000 11 108046360 synonymous variant A/G snv 0.68 0.59 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs6850
LOC105375259 ; PPIA
0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9
rs11212495
CUL5
1.000 11 108048172 intron variant A/G;T snv 1
rs1291142
SAMHD1
1.000 20 36896959 intron variant A/G;T snv 1
rs608114
LOC107986626
0.925 6 95928822 intron variant A/T snv 0.95 5
rs6723162 0.925 2 70875156 intergenic variant A/T snv 0.65 5
rs59440261
MICA
0.925 6 31403294 intron variant C/A snv 3.3E-02 5
rs7576600
LOC105374497
0.925 2 40840846 intergenic variant C/A;G snv 5
rs2294367
APOBEC3G
1.000 22 39083569 intron variant C/A;G snv 1
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs147879075
CCR5 ; CCR5AS
1.000 3 46373902 stop gained C/A;G;T snv 1.6E-05; 8.2E-06; 4.1E-06 1
rs146215995
TRIM5
1.000 11 5679850 missense variant C/A;T snv 8.0E-06; 9.5E-05 1