Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs1884614
LOC105372629
0.882 0.080 20 44351879 non coding transcript exon variant C/T snv 0.18 5
rs2293855
MTMR9
0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 5
rs3813929
HTR2C
0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5