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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861897, MYH7
(C1748Y)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1S
+8 more
GConflicting classifications of pathogenicity
MYH7
(T1019N)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GUncertain significance