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: rs13361707
rs13361707
0.882 0.120 5 40791782 intron variant C/T snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.780 1.000 11 2011 2018
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.720 1.000 3 2014 2018
dbSNP: rs154268
rs154268
0.925 0.080 5 40795766 intron variant C/T snv 0.69
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2018
dbSNP: rs6882903
rs6882903
0.925 0.080 5 40765760 intron variant A/C snv 2.7E-03
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2018
dbSNP: rs3805490
rs3805490
0.925 0.080 5 40792051 intron variant T/A snv 0.21
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs461404
rs461404
0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018