Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 8
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 8
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 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
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 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
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7