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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129389216, LOC129389217
+757 more
Copy number gain
See cases
GPathogenic
LOC129992665, LOC129992666
+103 more
Copy number loss
See cases
GPathogenic
AMBN, AMTN
+30 more
Copy number gain
See cases
GUncertain significance
ODAM
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
ODAM
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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