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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COQ2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
COQ2
Single nucleotide variant
(synonymous variant)
Coenzyme Q10 deficiency, primary, 1
+2 more
GBenign
LOC112997540, COQ2
(V66L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
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