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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130066383, LOC130066384
+464 more
Copy number gain
See cases
GPathogenic
LINC00266-1, MYT1
+1 more
Copy number gain
See cases
GLikely benign
MYT1
Single nucleotide variant
(intron variant)
not provided
GBenign
MYT1, PCMTD2
Copy number loss
See cases
GPathogenic
MYT1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
PPDPF, OPRL1
+35 more
Copy number loss
See cases
GPathogenic
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