MIR4725, microRNA 4725, 100616449

N. diseases: 4; N. variants: 1
Source: ALL
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: rs121224
rs121224 		0.851 0.080 17 31574981 intron variant G/C snv 0.66
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2016 2017
dbSNP: rs121224
rs121224 		0.851 0.080 17 31574981 intron variant G/C snv 0.66
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2016 2017
dbSNP: rs121224
rs121224 		0.851 0.080 17 31574981 intron variant G/C snv 0.66
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		Digestive System Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs121224
rs121224 		0.851 0.080 17 31574981 intron variant G/C snv 0.66
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2016 2016