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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MATN3, WDR35-DT
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
MATN3, WDR35-DT
(C321S)
Single nucleotide variant
(missense variant)
Connective tissue disorder
GUncertain significance
MATN3, WDR35-DT
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
MATN3, WDR35-DT
(T303M)
Single nucleotide variant
(missense variant)
Multiple epiphyseal dysplasia type 5
+3 more
GBenign
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