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: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.020 0.500 2 2012 2016
dbSNP: rs17033
rs17033
0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs283411
rs283411
0.925 0.080 4 99344800 intron variant C/A;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012