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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806067, RYR2
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC126806067, RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+5 more
GBenign
LOC126806067, RYR2
Single nucleotide variant
(synonymous variant)
RYR2-related condition
+5 more
GConflicting classifications of pathogenicity
LOC126806067, RYR2
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
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