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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS9-AS2, ARL6IP5
+234 more
Copy number loss
See cases
GPathogenic
LOC129936986, SLC25A26
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
GLikely benign