Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs998451
TMEM163
1.000 0.080 2 134671718 intron variant G/A;C snv 1
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs9966620
TTC39C
0.925 0.160 18 24100771 intron variant G/A snv 0.21 2
rs9966483
LOC643542
0.925 0.160 18 67783109 intron variant G/A;T snv 2
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs9958800
PHLPP1 ; LOC105372160
0.925 0.160 18 62773567 intron variant T/A snv 0.25 2
rs995447
ADGRL3
1.000 0.080 4 61952750 intron variant T/C snv 9.1E-02 1
rs994965583 1.000 0.080 15 79571143 intergenic variant C/T snv 1.1E-04 1
rs994411260
DNMT1
0.925 0.160 19 10194877 missense variant G/C snv 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs9940149
FAM234A
1.000 0.080 16 250642 intron variant G/A snv 0.32 1
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs9935401
FTO
0.925 0.120 16 53782926 intron variant G/A snv 0.40 3
rs9934336
SLC5A2
1.000 0.080 16 31484552 intron variant G/A snv 0.24 1
rs993380
SCD5
1.000 0.080 4 82663343 intron variant A/G snv 0.61 1
rs9931702
AKTIP
0.851 0.160 16 53492639 non coding transcript exon variant C/T snv 0.55 4
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs9926289
FTO
0.882 0.160 16 53786591 intron variant G/A snv 0.41 5
rs9917392
ARHGAP15
1.000 0.080 2 143138309 intron variant C/T snv 0.35 1
rs9915302
COX10
1.000 0.080 17 14085565 intron variant T/G snv 0.15 1
rs9911983
OSBPL7
1.000 0.080 17 47808390 synonymous variant C/T snv 0.50 0.58 1