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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GJA1
(K162N)
Single nucleotide variant
(missense variant)
Atrioventricular septal defect and common atrioventricular junction
+7 more
GLikely pathogenic
COL5A1
(P968fs)
Deletion
(frameshift variant)
Cutis laxa
+9 more
GLikely pathogenic