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: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 < 0.001 1 2006 2006
dbSNP: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1992 1992
dbSNP: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2007 2007
dbSNP: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2007 2007
dbSNP: rs587778720
rs587778720
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 < 0.001 1 2006 2006