rs7086803, VTI1A

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.720 1.000 3 2012 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.720 1.000 3 2012 2018
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.710 1.000 2 2015 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.700 1.000 1 2019 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.020 1.000 2 2015 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.010 1.000 1 2018 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.010 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
502 0.763 0.160 10 112738717 intron variant G/A snv 0.20 0.010 1.000 1 2018 2018