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
rs9972727 16 31137821 upstream gene variant A/C;G snv 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs983521
CADPS2
7 122434362 intron variant A/G snv 0.27 1
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs9806366 15 101262752 intergenic variant C/T snv 0.24 1
rs9794
PPARD
0.882 0.200 6 35428018 3 prime UTR variant G/A;C;T snv 4
rs9658668
CHGA
14 92932724 missense variant C/T snv 3.9E-04 1.2E-03 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs9634314
TCHP ; GIT2
12 109968581 intron variant G/A snv 0.20 1
rs9603502 13 31671676 intergenic variant C/A snv 0.32 1
rs9549328
MCF2L
13 112981842 intron variant C/T snv 0.21 2
rs9506725 13 21740007 regulatory region variant T/C snv 0.30 2
rs943580 1 230701298 upstream gene variant G/A snv 0.42 2
rs943346
SORBS1
10 95494548 intron variant C/G;T snv 2
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9330353
PCDH18
4 137518476 downstream gene variant T/A snv 0.55 2
rs9321485 6 135126635 intergenic variant T/C snv 0.29 3
rs9317097 13 22596235 upstream gene variant C/T snv 0.80 1
rs9291932 5 68747416 intergenic variant T/C snv 0.22 1
rs9291634
CPEB2 ; C1QTNF7-AS1
4 15019561 intron variant T/C snv 0.27 1