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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM135A
(Y158* +3 more)
Single nucleotide variant
(nonsense +1 more)
Histiocytoid cardiomyopathy
GLikely benign
NDUFB11
(R88*)
Single nucleotide variant
(nonsense)
Linear skin defects with multiple congenital anomalies 1
+3 more
GPathogenic