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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs2228314
SREBF2
0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs4844880
HSD11B1-AS1 ; HSD11B1
0.882 0.240 1 209697571 intron variant A/T snv 0.70 4