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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC9
(S1402C +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability and myopathy syndrome
+4 more
GUncertain significance
ABCC9
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1O
+6 more
GConflicting classifications of pathogenicity