RS267607053 SLC22A5

Health Risk Chr 5:132392489
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Renal carnitine transport defect
Inborn genetic diseases
Renal carnitine transport defect
Inborn genetic diseases
Other Variants in SLC22A5
rs72552727 rs1554087461 rs121908886 rs121908887 rs386134217 rs72552735 rs121908888 rs121908889 rs121908890 rs68018207
Ask Dr. Hemsworth about this variant