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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C2CD3
Single nucleotide variant
(intron variant +1 more)
Orofaciodigital syndrome type 14
+1 more
GUncertain significance
C2CD3
(P235L)
Single nucleotide variant
(missense variant)
Orofaciodigital syndrome type 14
+3 more
GBenign/Likely benign