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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPD1L
(I124V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+7 more
GConflicting classifications of pathogenicity
GPD1L
(E174K)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
GPD1L
(R231H)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+2 more
GUncertain significance
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