rs738722, CHEK2

N. diseases: 4
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 Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.882 0.120 22 28734024 intron variant T/C snv 0.67 0.810 1.000 2 2010 2012
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.882 0.120 22 28734024 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.882 0.120 22 28734024 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012
Secondary malignant neoplasm of lymph node
188 0.882 0.120 22 28734024 intron variant T/C snv 0.67 0.010 1.000 1 2012 2012