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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLA, RPL36A-HNRNPH2
(D313Y +1 more)
Single nucleotide variant
(missense variant +2 more)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity; other
GLA, RPL36A-HNRNPH2
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
GLA, RPL36A-HNRNPH2
Single nucleotide variant
(synonymous variant +2 more)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
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