SLC52A3, solute carrier family 52 member 3, 113278

N. diseases: 103; N. variants: 34
Disease: Squamous cell carcinoma of esophagus ×
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: rs13042395
rs13042395 		0.752 0.160 20 773867 intron variant C/T snv 5.9E-02
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.040 0.750 4 2015 2019
dbSNP: rs3746803
rs3746803 		1.000 0.080 20 763738 missense variant G/A;C snv 0.10; 1.2E-05
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2011 2016
dbSNP: rs3746802
rs3746802 		1.000 0.080 20 763664 missense variant T/C snv 0.10 9.3E-02
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3746804
rs3746804 		1.000 0.080 20 763771 missense variant G/A snv 0.19 0.19
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014