Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs1053874
DNASE1 ; TRAP1
0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 7
rs2230911
LOC105370032 ; P2RX7
0.807 0.360 12 121177328 missense variant C/G snv 0.14 0.12 6
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs104886308
COL4A5
0.851 0.160 X 108696350 missense variant G/A;C;T snv 2.2E-05 4
rs35366573
CD46
0.882 0.120 1 207785101 missense variant C/T snv 1.5E-02 1.5E-02 3
rs1556445736
COL4A5
0.925 0.200 X 108667167 synonymous variant A/G snv 5
rs10847697
SLC15A4
0.882 0.200 12 128814840 synonymous variant G/A snv 0.13 9.1E-02 3
rs1800897
PAX2
0.925 0.240 10 100809115 synonymous variant C/T snv 7.4E-02 0.13 2
rs2326369
MAVS
0.925 0.160 20 3862337 synonymous variant C/T snv 9.2E-02 0.11 2
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8