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: rs2228000
rs2228000
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 0.500 2 2014 2016
dbSNP: rs1870134
rs1870134
0.827 0.120 3 14178523 missense variant G/C;T snv 4.2E-02; 8.1E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2470352
rs2470352
0.925 0.080 3 14145330 missense variant A/G;T snv 1.7E-03; 0.15
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2607775
rs2607775
0.807 0.160 3 14178595 5 prime UTR variant C/G snv 0.42 0.43
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs535242729
rs535242729
0.925 0.080 3 14172913 missense variant G/A snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010