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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOZ3, MYOZ3-AS1
(L36P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MYOZ3, MYOZ3-AS1
(G131E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
MYOZ3, MYOZ3-AS1
(V133I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MYOZ3, MYOZ3-AS1
(S137G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MYOZ3, MYOZ3-AS1
(R182L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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