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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC16A1
(I325V)
Single nucleotide variant
(missense variant)
Metabolic myopathy due to lactate transporter defect
+4 more
GBenign/Likely benign
SLC16A1
Microsatellite
(intron variant)
Exercise-induced hyperinsulinism
+3 more
GBenign/Likely benign