Disease: Non-alcoholic Fatty Liver Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1420472625
MBOAT7
0.925 0.040 19 54178800 missense variant G/C snv 2
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs56225452
SLC27A5 ; LOC105372486 ; ZBTB45
0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800234
PPARA
0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3