RS606231311 SLC16A1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Monocarboxylate transporter 1 deficiency
autosomal dominant
Metabolic myopathy due to lactate transporter defect
Ketoacidosis due to monocarboxylate transporter-1 deficiency
Monocarboxylate transporter 1 deficiency
autosomal dominant
Metabolic myopathy due to lactate transporter defect
Ketoacidosis due to monocarboxylate transporter-1 deficiency
Other Variants in SLC16A1