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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DMD
(Q2366K +2 more)
Single nucleotide variant
(no sequence alteration +1 more)
Duchenne muscular dystrophy
+2 more
GBenign
DMD
(E432K +3 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity