Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063320
HLA-G
0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 10
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs175080
MLH3
0.776 0.240 14 75047125 missense variant G/A snv 0.40 0.43 9
rs3087386
REV1
0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs535915558
PMEL
0.827 0.120 12 55958494 missense variant C/T snv 2.0E-05 6
rs7208422
TMC8
0.807 0.120 17 78134494 missense variant A/C;T snv 4.0E-06; 0.51 6
rs807183
ATG4A
0.851 0.120 X 108094263 intron variant G/A snv 0.51 4
rs2232641
LIG4
0.851 0.160 13 108209297 missense variant T/C snv 1.5E-03 5.7E-04 4
rs8305
POLI
0.882 0.120 18 54294435 missense variant G/A snv 0.72 0.78 4
rs807181
PSMD10 ; ATG4A
0.851 0.120 X 108090354 intron variant G/C;T snv 4
rs3087399
REV1
0.882 0.120 2 99438696 missense variant T/C snv 0.13 0.17 4
rs311678
CGAS
1.000 0.040 6 73425293 synonymous variant C/T snv 0.71 0.72 2
rs6052130
MAVS
1.000 0.040 20 3863021 intron variant C/A snv 9.5E-02 2
rs17102999
MLH3
0.925 0.120 14 75046831 missense variant G/A snv 1.3E-02 9.8E-03 2
rs7133268
BRI3BP
1.000 0.040 12 125024464 intron variant A/G snv 0.48 1