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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTG1
(R210C)
Single nucleotide variant
(missense variant +1 more)
Baraitser-winter syndrome 2
GPathogenic
ACTG1
(T162M)
Single nucleotide variant
(missense variant +1 more)
Baraitser-winter syndrome 2
GUncertain significance
ACTG1
(H40Y)
Single nucleotide variant
(missense variant +1 more)
Baraitser-winter syndrome 2
GLikely pathogenic
ACTG1, LOC130061940
(P32H)
Single nucleotide variant
(missense variant +1 more)
Baraitser-winter syndrome 2
GLikely pathogenic
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