RS57262206 SLC22A5

Health Risk Chr 5:132369824
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Associated Conditions
Renal carnitine transport defect
SLC22A5-related disorder
Inborn genetic diseases
Renal carnitine transport defect
SLC22A5-related disorder
Inborn genetic diseases
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Carnitine levels — OR: 1.63 2E-42 PubMed
Other Variants in SLC22A5
rs72552727 rs1554087461 rs121908886 rs121908887 rs386134217 rs72552735 rs121908888 rs121908889 rs121908890 rs68018207
Ask Dr. Hemsworth about this variant