Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10759637
SLC31A1 ; CDC26
1.000 0.040 9 113262744 3 prime UTR variant A/C snv 0.47 2
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs104894816
GATA1
0.827 0.120 X 48792377 missense variant A/G snv 6
rs5030764
GP9
0.882 0.080 3 129061921 missense variant A/G snv 4.8E-04 7.4E-04 5
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs121908064
GP1BA ; CHRNE
1.000 0.080 17 4933367 missense variant A/G snv 3
rs4986910
CYP3A4
0.925 0.080 7 99760901 missense variant A/G snv 5.2E-03 5.1E-03 3
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs76600635
TLR1
0.925 0.040 4 38798702 missense variant A/G snv 8.2E-03 2.8E-03 3
rs10510050 10 118867050 intron variant A/G snv 0.52 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
rs794727505
GNE ; CLTA
9 36246181 missense variant A/G snv 8.0E-06 1
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs869320714
SLFN14
1.000 17 35557404 missense variant A/T snv 3
rs759838407
LIG4
0.925 0.160 13 108209756 frameshift variant AG/-;AGAG delins 3
rs1064797085
FLI1
1.000 11 128810620 frameshift variant ATTA/- delins 2
rs1523127
NR1I2
0.925 0.040 3 119782192 5 prime UTR variant C/A snv 0.48 3
rs17824620
RPH3A
12 112663189 intron variant C/A snv 0.26 2
rs9574547 13 80057282 intron variant C/A snv 0.17 1
rs143873938
FLNA
0.882 0.120 X 154365245 missense variant C/A;G;T snv 3.1E-03 4