Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs12268840
MGMT
0.827 0.200 10 129527035 intron variant C/T snv 0.22 6