Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs11697186
DDRGK1
1.000 0.080 20 3204477 intron variant A/C;T snv 7.0E-02 1
rs6139030
ITPA
1.000 0.080 20 3207087 upstream gene variant T/C snv 8.6E-02 1
rs965469
C20orf194
1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs8103142
IFNL3
0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4
rs2230201
C3
0.882 0.200 19 6713280 synonymous variant C/G;T snv 0.19 3
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs2779180
PLIN3
1.000 0.080 19 4841139 intron variant A/G snv 0.37 1
rs28416813
IFNL3
1.000 0.080 19 39245004 5 prime UTR variant C/G snv 0.31 0.39 1