Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7712322
POLR3G
1.000 0.080 5 90482078 intron variant C/A;T snv 1
rs78900671
COL22A1
1.000 0.080 8 138653967 intron variant G/A;C snv 1
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs148314165 0.925 0.160 6 137908902 intergenic variant T/- delins 2.0E-02 3
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs76844316
BTLA
1.000 0.080 3 112469762 missense variant T/G snv 2.4E-02 2.2E-02 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs117648444
IFNL4
0.882 0.160 19 39247938 missense variant G/A snv 0.25 8.1E-02 3
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs3806798
IL15
0.925 0.080 4 141636126 upstream gene variant T/A snv 8.7E-02 2
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs61886277
PLCE1
1.000 0.080 10 94012060 intergenic variant C/T snv 0.19 1
rs2853953 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 1
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4