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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TYROBP
(P109L +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
TYROBP
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GBenign/Likely benign
TYROBP
Single nucleotide variant
(intron variant)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
+1 more
GBenign
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