rs9841504, ZBTB20

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.
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.827 0.120 3 114643917 intron variant C/G;T snv 0.720 0.667 3 2011 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.827 0.120 3 114643917 intron variant C/G;T snv 0.720 0.667 3 2011 2016
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.827 0.120 3 114643917 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.827 0.120 3 114643917 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.827 0.120 3 114643917 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.827 0.120 3 114643917 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.827 0.120 3 114643917 intron variant C/G;T snv 0.010 1.000 1 2017 2017