Source: ALL

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: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2014 2014
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		0.010 1.000 1 2018 2018
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
Carcinoma in situ of uterine cervix 		0.010 1.000 1 2018 2018
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 1.000 1 2014 2014
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
Cervical Squamous Cell Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs246079
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2018 2018