Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 10
rs807181
PSMD10 ; ATG4A
0.851 0.120 X 108090354 intron variant G/C;T snv 4
rs807183
ATG4A
0.851 0.120 X 108094263 intron variant G/A snv 0.51 4
rs6052130
MAVS
1.000 0.040 20 3863021 intron variant C/A snv 9.5E-02 2
rs7133268
BRI3BP
1.000 0.040 12 125024464 intron variant A/G snv 0.48 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
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