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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS10
(R1001H +1 more)
Single nucleotide variant
(missense variant)
Weill-Marchesani syndrome 1
GUncertain significance
ADAMTS10
(A365T +1 more)
Single nucleotide variant
(missense variant)
Weill-Marchesani syndrome 1
GUncertain significance