SLC6A19, solute carrier family 6 member 19, 340024

N. diseases: 54; N. variants: 18
Disease: IMINOGLYCINURIA, DIGENIC ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3148959
Disease: IMINOGLYCINURIA, DIGENIC
IMINOGLYCINURIA, DIGENIC 		0.400 Biomarker disease GENOMICS_ENGLAND A novel missense mutation in the SLC6A19 gene in a Chinese family with Hartnup disorder. 19335424 2009
CUI: C3148959
Disease: IMINOGLYCINURIA, DIGENIC
IMINOGLYCINURIA, DIGENIC 		0.400 CausalMutation disease CLINVAR