Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs10827209
NRP1
10 33198261 intron variant A/C snv 0.23 2
rs2885296
UGT1A8 ; UGT1A9 ; UGT1A10 ; UGT1A5 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A4
2 233750415 intron variant A/C snv 0.30 2
rs79666748 18 43280443 upstream gene variant A/C snv 7.0E-02 2
rs9341664 6 77375469 intergenic variant A/C snv 0.51 2
rs6575267
RIN3
14 92580988 intron variant A/C snv 0.63 1
rs4802
SNORD14E ; HSPA8
11 123057914 synonymous variant A/C;G snv 4.1E-06; 0.32 2
rs7109445
CLMP
11 123094779 intron variant A/C;G snv 2
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs10892961
CLMP
11 123093392 intron variant A/C;G;T snv 2
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs5010528
HLA-B ; HLA-C
0.827 0.240 6 31273255 intron variant A/G snv 0.15 9
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs40837
IL27
0.925 0.120 16 28499524 3 prime UTR variant A/G snv 0.43 5
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs11695484
DNAJB3 ; UGT1A3 ; UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A5
2 233745803 intron variant A/G snv 0.30 3
rs10054178
C5orf17
5 24059742 intron variant A/G snv 7.5E-02 2
rs11218976
CLMP
11 123090950 intron variant A/G snv 0.41 2
rs11926663
IGSF11
3 119125638 intron variant A/G snv 1.8E-02 2
rs4936767 11 123047451 upstream gene variant A/G snv 0.34 2
rs7035473
OLFM1
9 135121519 downstream gene variant A/G snv 0.11 2
rs7121616
CLMP
11 123095918 intron variant A/G snv 0.41 2