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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTDP1
(S61A)
Single nucleotide variant
(missense variant)
Congenital cataracts-facial dysmorphism-neuropathy syndrome
+2 more
GBenign
CTDP1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GBenign