Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs199734815
rs199734815
MGMT ; LOC105378560
1.000 0.080 10 129708022 missense variant C/T snv 6.0E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs199734815
rs199734815
MGMT ; LOC105378560
1.000 0.080 10 129708022 missense variant C/T snv 6.0E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs199734815
rs199734815
MGMT ; LOC105378560
1.000 0.080 10 129708022 missense variant C/T snv 6.0E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 < 0.001 1 2019 2019