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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC110120630, LOC111429626
+608 more
Copy number gain
See cases
GPathogenic
FBLN2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FBLN2
(T854A +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
FBLN2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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