Disease: Hepatitis C
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10945859
PRKN
0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs1346044973
TERT
0.851 0.160 5 1294158 missense variant G/A snv 1.1E-05 4
rs2596538
MICA ; MICA-AS1
0.851 0.160 6 31400855 intron variant G/A snv 0.41 5
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20