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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRND
(R43W)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
CHRND
(A46T)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
CHRND
(L73P)
Single nucleotide variant
(missense variant +2 more)
Lethal multiple pterygium syndrome
+1 more
GUncertain significance
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