Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 6
rs9899375
CHD3
1.000 0.080 17 7908297 intron variant C/T snv 8.1E-03 2
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs976683
NLGN1
3 173767581 intron variant C/T snv 0.62 1
rs9693999
SLC7A13
8 86214418 missense variant C/T snv 9.0E-03 3.3E-02 1
rs966221
PDE4D
1.000 0.080 5 60206693 intron variant A/G snv 0.57 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9604365 13 111922883 intergenic variant G/A snv 0.82 1
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs9574
PROCR ; MMP24-AS1-EDEM2
1.000 0.080 20 35176829 3 prime UTR variant C/A;G;T snv 1.1E-03; 0.55 2
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9526212
LRCH1
1.000 0.080 13 46651610 intron variant A/G snv 0.74 2
rs9521634
COL4A1
13 110181552 intron variant T/A;C snv 1
rs9472313 6 44624969 regulatory region variant G/A snv 0.26 1
rs9467504
CARMIL1 ; CMAHP
6 25414097 intron variant A/G snv 0.18 1
rs9465922
CDKAL1
6 20865366 intron variant C/A snv 0.92 1
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs9345396 6 93779501 regulatory region variant C/T snv 1.7E-02 1
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs934075
PTCSC3
14 36169016 intron variant G/A snv 0.62 1