Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 5
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs12447924
CETP
1.000 16 56960280 upstream gene variant C/T snv 0.76 3
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 3
rs7946
PEMT
0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 6
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs2072906
PNPLA3
0.851 0.160 22 43937292 intron variant A/G snv 0.25 0.20 4
rs2072907
PNPLA3
0.882 0.120 22 43936773 intron variant C/G snv 0.20 3