Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
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
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
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8