Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033623
SH2D1A ; STAG2
0.925 0.080 X 124365786 stop gained C/T snv 3
rs2427870 X 136581905 upstream gene variant C/T snv 0.52 1
rs34688635
NOX1
X 100850206 missense variant C/T snv 1.9E-02 2.0E-02 1
rs747581281
CFP
X 47624319 missense variant G/C snv 3.3E-05 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 9
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs2412971
HORMAD2
0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs142430606
IL17REL
0.925 0.040 22 49998059 missense variant G/A;T snv 1.1E-02; 4.4E-06 3
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 3
rs35873774
XBP1
0.925 0.040 22 28795944 intron variant A/G snv 4.6E-02 3
rs5763767
HORMAD2
0.925 0.040 22 30097893 intron variant G/A;T snv 3
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 2
rs130555
SYN3
1.000 0.040 22 32787803 intron variant C/T snv 0.77 2
rs200958270
IL17REL
1.000 0.040 22 49999850 missense variant T/C snv 1.1E-02 6.1E-03 2
rs2412973
HORMAD2
1.000 0.080 22 30133642 intron variant C/A snv 0.54 2
rs713875
HORMAD2 ; LOC105372988
1.000 0.040 22 30196498 intron variant C/G snv 0.47 2
rs1003342
HORMAD2
22 30174033 intron variant A/G snv 0.45 1
rs2412970
HORMAD2
22 30090837 intron variant A/G snv 0.55 1
rs4821558
CSF2RB
22 36912743 upstream gene variant T/C snv 0.20 1
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9