Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs997509
ENPP1
0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs945508
ARHGEF11 ; MIR765 ; LRRC71
1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 3
rs935907949
SH2B1
16 28867355 missense variant C/T snv 7.0E-06 1
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs867232360
GCK
1.000 0.040 7 44145552 missense variant C/T snv 3
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs78655421
CFTR
0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs775018856
SLC2A4
1.000 0.080 17 7283304 synonymous variant G/A snv 2.8E-05 1.4E-05 2
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs760555162
GAPDH
1.000 0.080 12 6537178 synonymous variant G/A snv 4.0E-06 2
rs75527207
CFTR
0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs72551362
PPARG
0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 4
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs587783672
KCNJ11
0.882 0.080 11 17387413 missense variant C/T snv 4.0E-06 5
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs495490
CDKN2B-AS1 ; CDKN2B
1.000 0.080 9 22010413 intron variant A/G snv 6.8E-02 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21