Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
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
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 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
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
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8