SLC39A4, solute carrier family 39 member 4, 55630

N. diseases: 87; N. variants: 12
Disease: Zinc deficiency ×
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: rs121434292
rs121434292 		0.925 0.120 8 144416001 missense variant G/A;T snv 9.9E-06
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		Nutritional and Metabolic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs534850657
rs534850657 		0.925 0.120 8 144413980 missense variant A/G snv
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs782427403
rs782427403 		0.925 0.120 8 144413980 frameshift variant A/- del 4.2E-06 7.0E-06
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014