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
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs7946
PEMT
0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 6
rs4808199
GATAD2A ; MIR640
1.000 0.040 19 19434290 intron variant G/A;T snv 0.19 5
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 4
rs3135507
ZPR1 ; APOA5
0.925 0.120 11 116790772 missense variant C/T snv 5.0E-02 5.5E-02 3
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2