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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYO9B
(G283V)
Single nucleotide variant
(missense variant)
Muscle weakness
+1 more
GLikely pathogenic
COL6A2
Single nucleotide variant
(intron variant)
Collagen 6-related myopathy
+10 more
GPathogenic/Likely pathogenic
FHL1
(H55Y +2 more)
Single nucleotide variant
(missense variant +1 more)
Muscle weakness
GUncertain significance
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