RS606231310 SLC16A1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Monocarboxylate transporter 1 deficiency
autosomal recessive
Exercise-induced hyperinsulinism
Monocarboxylate transporter 1 deficiency
autosomal recessive
Exercise-induced hyperinsulinism
Other Variants in SLC16A1