Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9841504
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.720 0.667 2 2011 2016
dbSNP: rs9841504
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.720 0.667 2 2011 2016
dbSNP: rs9841504
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia 		0.010 1.000 1 2017 2017
dbSNP: rs9841504
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs9841504
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2017 2017
dbSNP: rs9841504
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2017 2017