Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs773919809
MGMT
0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 13
rs1625649
MGMT
0.882 0.080 10 129466667 upstream gene variant A/C snv 0.61 3
rs199734815
MGMT ; LOC105378560
1.000 0.080 10 129708022 missense variant C/T snv 6.0E-05 3
rs2308318
MGMT
0.925 0.080 10 129766851 missense variant G/A snv 6.2E-04 1.3E-03 2