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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH3
(R1137C)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and variable skeletal fusions syndrome 1B
+6 more
GBenign/Likely benign
MYH3
Single nucleotide variant
(synonymous variant)
Freeman-Sheldon syndrome
+6 more
GBenign
MYH3
Single nucleotide variant
(synonymous variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
+6 more
GBenign/Likely benign
MYH3
(V40M)
Single nucleotide variant
(missense variant)
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
+4 more
GUncertain significance
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