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: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2013 2013
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs7164773
rs7164773
0.790 0.240 15 60775749 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2017 2017