RS72552732 SLC22A5

Health Risk Chr 5:132392484
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What This Variant Does
"CLNSIG=5
Associated Conditions
Renal carnitine transport defect
Inborn genetic diseases
Decreased circulating carnitine concentration
SLC22A5-related disorder
Renal carnitine transport defect
Inborn genetic diseases
Decreased circulating carnitine concentration
SLC22A5-related disorder
Other Variants in SLC22A5
rs72552727 rs1554087461 rs121908886 rs121908887 rs386134217 rs72552735 rs121908888 rs121908889 rs121908890 rs68018207
Ask Dr. Hemsworth about this variant