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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS10
Single nucleotide variant
(intron variant)
Weill-Marchesani syndrome 1
+2 more
GBenign/Likely benign
ADAMTS10
(P18R)
Single nucleotide variant
(missense variant +1 more)
Weill-Marchesani syndrome
+2 more
GBenign/Likely benign