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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIP12
(H1617Y +11 more)
Single nucleotide variant
(missense variant)
Clark-Baraitser syndrome
GUncertain significance
TRIP12
(Y1399C +11 more)
Single nucleotide variant
(missense variant)
Clark-Baraitser syndrome
GUncertain significance
TRIP12
(P1360L +11 more)
Single nucleotide variant
(missense variant)
Clark-Baraitser syndrome
GLikely pathogenic
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