SLC6A19, solute carrier family 6 member 19, 340024

N. diseases: 54; N. variants: 18
Disease: Hypertensive disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.210 GeneticVariation group LHGDN These findings suggest that the rare SLC6A19-MS7 allele may be a risk factor for hypertension. 18671945 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.210 GeneticVariation group BEFREE These findings suggest that the rare SLC6A19-MS7 allele may be a risk factor for hypertension. 18671945 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.210 Biomarker group RGD High-salt intake and the renal expression of amino acid transporters in spontaneously hypertensive rats. 17264310 2007