Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs290481
rs290481
0.827 0.200 10 113164066 intron variant C/T snv 0.20
Adenocarcinoma of the gastroesophageal junction
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
Adenocarcinoma of the gastroesophageal junction
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019