Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs3764880
TLR8-AS1 ; TLR8
0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs3853839
TLR7
0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 10
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs3764879
TLR8 ; TLR8-AS1
0.807 0.320 X 12906578 intron variant C/G snv 0.30 6
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs1616583 0.882 0.120 X 12891363 downstream gene variant C/G snv 0.24 3
rs1634323
TLR7
0.882 0.200 X 12870008 intron variant A/G snv 0.11 3
rs179010
TLR7
0.882 0.200 X 12884766 intron variant T/C snv 3
rs179019
TLR7
0.882 0.160 X 12871850 intron variant A/C;T snv 3
rs2280964
CXCR3
0.882 0.200 X 71618204 intron variant C/A;G;T snv 3
rs2239464
MECP2
0.925 0.120 X 154082978 intron variant G/A snv 0.34 2
rs2269368
ARHGAP4
0.925 0.120 X 153924366 intron variant C/G;T snv 2
rs34334103
CXCR3
0.925 0.160 X 71618225 intron variant C/T snv 1.2E-02 2
rs10127175
IRAK1
1.000 0.080 X 154018721 missense variant A/T snv 5.1E-03 1.8E-02 1
rs1634318 1.000 0.080 X 12891359 downstream gene variant A/G snv 0.24 1
rs1734787
MECP2
1.000 0.080 X 154059995 non coding transcript exon variant A/C snv 0.17 1
rs1734791
MECP2
1.000 0.080 X 154065469 intron variant A/T snv 0.22 1
rs1734792
MECP2
1.000 0.080 X 154075609 intron variant C/A snv 0.21 1
rs2049995
SH2D1A ; STAG2
1.000 0.080 X 124366141 intron variant T/G snv 1