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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130061940, ACTG1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign/Likely benign
ACTG1, LOC130061940
Single nucleotide variant
(synonymous variant +1 more)
Baraitser-winter syndrome 2
+4 more
GBenign/Likely benign