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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH3
(Y583S)
Single nucleotide variant
(missense variant)
Freeman-Sheldon syndrome
GPathogenic
MYH3
(T178I)
Single nucleotide variant
(missense variant)
MYH3-Related Disorders
+3 more
GPathogenic