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
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1420472625
MBOAT7
0.925 0.040 19 54178800 missense variant G/C snv 2
rs1800234
PPARA
0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
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