Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs17525495
LTA4H
0.882 0.080 12 96035599 5 prime UTR variant G/A snv 9.9E-02 4
rs3870369 1.000 0.080 6 153261855 intron variant T/G snv 0.65 2
rs116264669
CCDC33
15 74309203 intron variant G/A snv 3.4E-02 1
rs72739603
LOC105376035
9 37382234 downstream gene variant G/A snv 6.7E-02 1
rs2309554
TENM3-AS1 ; TENM3
4 181902651 intron variant G/A;T snv 1
rs12081070
UBE2U
1 64215092 intron variant G/A snv 0.47 1