Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs9988450
DOCK7
1 62458777 non coding transcript exon variant C/T snv 0.39 3
rs9988442
TMIGD3 ; RAP1A
1 111554040 intron variant C/A;T snv 1
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs9963938 18 22330221 intergenic variant C/G;T snv 1
rs995000
DOCK7
1 62641855 intron variant C/T snv 0.34 4
rs9949617
TMEM241
18 23299253 intron variant C/T snv 0.22 2
rs9948087
THOC1
18 268992 non coding transcript exon variant C/A snv 0.24 1
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9932251
NFATC3
16 68097829 intron variant G/A snv 0.19 1
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs9912177
ITGB3
17 47285851 intron variant A/T snv 6.4E-03 3
rs9892506 17 42752474 upstream gene variant A/G snv 0.13 1
rs9863753
STAB1
3 52495883 intron variant A/C;G;T snv 2
rs9838771
TGFBR2 ; LOC105377016
3 30657290 intron variant G/A snv 2.5E-02 3
rs9817452 3 157077625 upstream gene variant G/T snv 0.31 2
rs9804646
APOA5
11 116794363 upstream gene variant C/T snv 0.17 3
rs9715911 5 156967430 upstream gene variant G/A snv 0.60 1
rs9687833
C5orf67
1.000 0.080 5 56565774 intron variant G/A snv 0.21 3
rs9686661
C5orf67
1.000 0.080 5 56565959 intron variant C/T snv 0.20 3
rs9658736
FAS
10 89004160 intron variant T/C snv 9.4E-03 3