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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM1L
(T102M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GUncertain significance
DNM1L
Single nucleotide variant
(intron variant)
Optic atrophy 5
+3 more
GBenign/Likely benign
DNM1L
Single nucleotide variant
(splice donor variant)
not provided
+2 more
GLikely pathogenic
DNM1L
Deletion
(intron variant)
not provided
+3 more
GBenign/Likely benign
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