RS28383481 SLC22A5

Health Risk Chr 5:132393687 snv missense variant

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What This Variant Does

"minor allele should be reclassified as benign according to

Associated Conditions

Renal carnitine transport defect

Population Frequencies

gnomAD ALL

0.5%

1kG AFR

100%

1kG ALL

99.9%

1kG AMR

0.7%

1kG EAS

100%

1kG EUR

0.2%

1kG SAS

100%

Other Variants in SLC22A5