Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs17446593 1.000 0.080 13 40553948 intron variant A/G snv 0.19 2
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
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
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs945508
ARHGEF11 ; MIR765 ; LRRC71
1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs1527483
CD36
1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 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
rs78655421
CFTR
0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs75527207
CFTR
0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249