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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTSL2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
ADAMTSL2
Single nucleotide variant
(synonymous variant)
Geleophysic dysplasia 1
GUncertain significance
ADAMTSL2
(T679S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
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