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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129936729, NDUFAF3
(S9I)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
LOC129936729, NDUFAF3
(P25L)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
LOC129936729, NDUFAF3
Single nucleotide variant
(intron variant)
not specified
+1 more
GLikely benign
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