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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806068, RYR2
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GConflicting classifications of pathogenicity
LOC126806068, RYR2
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign