Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 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
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs1554483
CLOCK
0.882 0.160 4 55455650 intron variant C/G snv 0.33 5