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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CPT2, LOC129930561
(S38fs)
Microsatellite
(frameshift variant)
Carnitine palmitoyltransferase II deficiency
+5 more
GPathogenic/Likely pathogenic
CPT2, LOC129930561
(P50H)
Single nucleotide variant
(missense variant)
Chronic pain
+13 more
GPathogenic