Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12614
CYP21A2 ; CFB
0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 5
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs3759333
LTBR
0.882 0.120 12 6382781 intron variant C/G;T snv 3
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs7756516
HLA-DQB2
0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 4
rs61886277
PLCE1
1.000 0.080 10 94012060 intergenic variant C/T snv 0.19 1
rs9287655
NBAS
1.000 0.080 2 15245360 intron variant C/T snv 0.45 1
rs1054690270
LOC101928953 ; GPT
0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs1419881
TCF19
0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 4