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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOM1
(G1585R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MYOM1
(A1578T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MYOM1
(R351Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MYOM1
(I328del)
Microsatellite
(inframe_deletion)
not provided
+1 more
GConflicting classifications of pathogenicity
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