rs6458238, PGC

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.882 0.080 6 41749967 intron variant G/A;C snv 0.040 1.000 4 2013 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.882 0.080 6 41749967 intron variant G/A;C snv 0.030 1.000 3 2013 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.882 0.080 6 41749967 intron variant G/A;C snv 0.030 1.000 3 2013 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.882 0.080 6 41749967 intron variant G/A;C snv 0.010 1.000 1 2016 2016