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
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16