Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs534356339
CCSER1
4 91335712 intron variant GAT/- del 3.4E-03 1
rs144582188 4 45163634 intergenic variant CTT/- delins 2
rs397778224 16 19912366 regulatory region variant -/C delins 0.21 2
rs11288989
NIPBL
5 37043527 intron variant AAA/-;A;AA;AAAA;AAAAA delins 1
rs143814719
LOC105372155
18 60300038 intron variant AAG/- delins 0.21 1
rs151204774 11 21580341 downstream gene variant AATT/- delins 7.4E-02 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5