Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6458238
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		0.040 1.000 4 2013 2016
dbSNP: rs6458238
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.030 1.000 3 2013 2016
dbSNP: rs6458238
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.030 1.000 3 2013 2016
dbSNP: rs6458238
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2016 2016