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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CA7
(Y22F)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
CA7
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CA7
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
B3GNT9, BEAN1
+25 more
Deletion
not provided
GPathogenic
CYB5B, DDX19A
+127 more
Deletion
Dyskeratosis congenita, autosomal dominant 6
GUncertain significance
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