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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS10
(S1088G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ADAMTS10
(G1065S +1 more)
Single nucleotide variant
(missense variant)
Weill-Marchesani syndrome
+2 more
GBenign/Likely benign
ADAMTS10
(V673I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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