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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMELX, ANOS1
+152 more
Copy number gain
See cases
GPathogenic
ACE2, ACE2-DT
+168 more
Copy number gain
See cases
GPathogenic
CLDN34, GPR143
+13 more
Copy number gain
See cases
GUncertain significance
GPR143, LOC130067929
Single nucleotide variant
(intron variant)
not provided
GBenign
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