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
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
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
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
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
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs2297627
FOXO1
0.925 0.120 13 40659794 intron variant A/G snv 0.41 3
rs11061946
ADIPOR2
1.000 0.080 12 1719361 intron variant C/T snv 6.8E-02 2
rs11061973
ADIPOR2
1.000 0.080 12 1756770 intron variant G/A snv 0.12 2
rs1527483
CD36
1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 2
rs17446593 1.000 0.080 13 40553948 intron variant A/G snv 0.19 2
rs3731201
CDKN2A
1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs495490
CDKN2B-AS1 ; CDKN2B
1.000 0.080 9 22010413 intron variant A/G snv 6.8E-02 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614