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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYSF
(V119fs +1 more)
Deletion
(frameshift variant)
Miyoshi muscular dystrophy 1
+4 more
GPathogenic
DYSF
(F1853L +13 more)
Single nucleotide variant
(missense variant)
Qualitative or quantitative defects of dysferlin
GPathogenic