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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTG1
(R335H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GPathogenic/Likely pathogenic
ACTG1
(D56N)
Single nucleotide variant
(missense variant +1 more)
Baraitser-winter syndrome 2
GUncertain significance
ACTG1
(G42S)
Single nucleotide variant
(missense variant +1 more)
Baraitser-winter syndrome 2
GUncertain significance
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