Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs762513613
FCGR2C
0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs765502022
UGT2B7
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs28399499
CYP2B6
0.827 0.280 19 41012316 missense variant T/C snv 5.1E-03 2.2E-02 6
rs1799972
OPRM1
0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs14158
LDLR
0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs1188975135
APOBEC3C ; APOBEC3F
0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs10336
LOC101928809 ; CXCL9
0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs11045819
SLCO1B1
0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 4
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs4619915
CXCL11 ; ART3
0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs10892151
DSCAML1 ; LOC105369515
1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs1194919682
CXCR4 ; LOC112268426
0.925 0.040 2 136115158 missense variant A/G snv 2
rs57302492
CD207
1.000 2 70831099 missense variant T/A snv 7.0E-02 8.9E-02 1
rs1276738522
CD9 ; LOC105369625
1.000 12 6232664 start lost A/G snv 4.9E-06 1
rs749569169
CHN2 ; LOC107986700
1.000 7 29512676 missense variant A/G snv 4.0E-06 1
rs1272938495
CXCR4 ; LOC112268426
1.000 2 136115225 missense variant G/A snv 4.0E-06 7.0E-06 1
rs774027752
CYP2A6
1.000 19 40845472 missense variant T/C snv 8.0E-06 1.4E-05 1