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
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs7269320
MAVS
20 3865750 missense variant C/T snv 0.16 0.21 1
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs179363879
AIRE
0.925 0.160 21 44286092 missense variant T/C snv 3
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs781522558
STAT2
1.000 12 56346844 stop gained G/C;T snv 4.0E-06 2
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs139226823
CXCR3
X 71616597 missense variant C/G;T snv 5.5E-06; 5.7E-04 1
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15