Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 6
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 5
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 5
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5