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Links from PMC

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XYLT1
(R406W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
XYLT1
(A115S)
Single nucleotide variant
(missense variant)
Desbuquois dysplasia 2
+2 more
GBenign
XYLT2
(T801R)
Single nucleotide variant
(missense variant +1 more)
Osteogenesis imperfecta
+2 more
GBenign
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