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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLDN10
(N48H)
Single nucleotide variant
(missense variant +1 more)
HELIX syndrome
GLikely pathogenic
CLDN10
(W145* +2 more)
Single nucleotide variant
(nonsense)
HELIX syndrome
GPathogenic