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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COQ7, COQ7-DT
+1 more
(C3S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
COQ7, COQ7-DT
+1 more
(G5R)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
COQ7, COQ7-DT
+1 more
(A6V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
COQ7, LOC130058587
(A19S)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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