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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTN
(R9744C +2 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive limb-girdle muscular dystrophy type 2J
+9 more
GConflicting classifications of pathogenicity
CACNB2
Single nucleotide variant
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity