Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 7
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 7
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 7
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 7
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 5
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 5
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 5
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 5
rs4704220
CERT1
5 75461731 intron variant G/A snv 0.55 5
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 5
rs6013029
CTNNBL1
0.882 0.160 20 37771178 intron variant G/T snv 0.12 5
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 5