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: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
0.700 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
0.645 0.440 17 7674947 missense variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2016 2016