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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAM10, ALDH1A2
+287 more
Copy number loss
See cases
GPathogenic
LEO1
(S447P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LEO1
(P433R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LEO1
(L411I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LEO1
(R411G)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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