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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARMC10, ATXN7L1
+86 more
Copy number loss
See cases
GPathogenic
PSMC2, SLC26A5
Single nucleotide variant
(intron variant)
not provided
GBenign
PSMC2, SLC26A5
Single nucleotide variant
(intron variant)
not provided
GBenign
PSMC2, SLC26A5
Single nucleotide variant
(intron variant)
not provided
GLikely benign
PSMC2, SLC26A5
(V122fs)
Duplication
(frameshift variant +1 more)
not provided
GUncertain significance
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