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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COQ2
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
COQ2, LOC112997540
(V66L +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
COQ2, LOC112997540
(R22*)
Single nucleotide variant
(nonsense)
Multiple system atrophy 1, susceptibility to
+4 more
GBenign/Likely benign
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