rs1989969, VDR

N. diseases: 8
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.
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2017 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2013 2013
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2017 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2013 2013
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2014 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2013 2013
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 0.010 1.000 1 2014 2014