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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH3
(L1344P)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
GUncertain significance
MYH3
(T333R)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
GLikely pathogenic
MYH3
(F287V)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
GLikely pathogenic
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