Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7