Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs2854116
APOC3
0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6