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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTR2, AFTPH
+173 more
Copy number loss
See cases
GPathogenic
LOC129933945, SLC1A4
Deletion
(intron variant)
not provided
GBenign
LOC129933945, SLC1A4
Deletion
(intron variant)
not provided
GBenign
LOC129933945, SLC1A4
Single nucleotide variant
(intron variant)
not provided
GBenign
LOC129933945, SLC1A4
Single nucleotide variant
(intron variant)
not provided
GBenign
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