Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs938448224
STAT5B
0.807 0.160 17 42207711 missense variant T/G snv 7.0E-06 7
rs752317734
DECR1
0.851 0.120 8 90020913 missense variant T/C snv 4.9E-06 5
rs145036301
ECSIT
0.851 0.120 19 11513899 missense variant A/G snv 2.7E-03 9.4E-04 5
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs61733010
AKR1A1
0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 2
rs753716491
GNAQ
1.000 0.120 9 77922196 missense variant T/A snv 2
rs758837678
NBN ; DECR1
0.925 0.120 8 90001503 missense variant C/T snv 2
rs753861648
NCR1
1.000 0.120 19 54906742 missense variant G/C snv 4.0E-06 2
rs1442744764
NOTCH1
1.000 0.120 9 136496490 missense variant G/A snv 4.2E-06 1