rs2107301, VDR

N. diseases: 7
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.
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2014 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2014 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2014 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2007 2007
melanoma
CUI: C0025202
Disease: melanoma
515 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1 2012 2012
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2007 2007
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2014 2014