Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
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
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9846911 3 187500548 intergenic variant A/G snv 0.47 2
rs974453
SLCO1C1
1.000 0.080 12 20737008 intron variant A/G;T snv 3
rs9677
VIPR1
0.925 0.080 3 42537370 3 prime UTR variant C/T snv 0.39 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9640883
LOC105375519
0.882 0.120 7 134431881 intron variant G/A snv 0.21 4
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs952635
PDE4B
1.000 0.040 1 66226202 intron variant C/G;T snv 2
rs952497863
HNF4A
0.925 0.080 20 44414511 missense variant C/T snv 4
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs950561906
SDS
0.925 0.120 12 113398775 missense variant T/C snv 8.0E-06 7.0E-06 3
rs9470794
ZFAND3
0.925 0.080 6 38139068 intron variant T/C snv 0.12 3
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs931891
LINC00923
1.000 0.040 15 97749977 intron variant C/A snv 6.4E-02 2
rs9299870
MGMT
1.000 0.040 10 129471045 intron variant C/A;G;T snv 2
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs9273643
HLA-DQB1
0.925 0.120 6 32661407 missense variant A/G snv 3
rs9267551
CLIC1 ; DDAH2
0.807 0.160 6 31730180 5 prime UTR variant C/G;T snv 7