Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs6667202
IL19
0.882 0.120 1 206783747 intron variant C/A;T snv 4
rs11789898
BRD3
9 134060541 intron variant G/T snv 0.14 3
rs2071346
MYC ; CASC11
0.925 0.160 8 127736777 intron variant G/T snv 7.1E-02 3
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs7694379 1.000 4 87265357 intron variant G/A snv 0.40 3
rs7729269
MCC
0.925 0.040 5 113384697 intron variant T/C snv 0.17 3
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs17824620
RPH3A
12 112663189 intron variant C/A snv 0.26 2
rs1800812
PDGFRA
1.000 0.080 4 54228462 intron variant G/C;T snv 2
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs10510050 10 118867050 intron variant A/G snv 0.52 1
rs11598702
NT5C2
10 103138228 intron variant T/C;G snv 1
rs3786136
RPA1
17 1869979 intron variant G/A snv 0.24 1
rs4694362
DCK
4 71028147 intron variant C/T snv 0.49 1
rs5030437
TRAF6
11 36503205 intron variant A/G snv 0.78 1
rs5030470
TRAF6
11 36493896 intron variant A/G snv 0.12 1
rs9574547 13 80057282 intron variant C/A snv 0.17 1
rs80338701
PMM2
0.776 0.360 16 8811088 stop gained C/A;T snv 4.4E-05; 5.4E-06 14
rs138924661
DGKE ; TRIM25
0.807 0.120 17 56848773 stop gained G/A snv 9.1E-05 1.5E-04 9
rs104894419
LIG4
0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs121909752
SEPT5-GP1BB ; GP1BB ; SEPTIN5
0.925 0.080 22 19723980 stop gained G/A;C snv 7.5E-06 4
rs1569061768
RUNX1
1.000 0.120 21 34859477 stop gained G/A snv 2