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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A4
(A123D)
Single nucleotide variant
(missense variant)
Progressive sensorineural hearing impairment
+9 more
GPathogenic/Likely pathogenic
PRKAG2
(P197R +2 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+9 more
GUncertain significance