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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BCS1L
(R56*)
Single nucleotide variant
(nonsense +3 more)
BCS1L-Related Disorders
+5 more
GPathogenic
BCS1L
Single nucleotide variant
(synonymous variant +3 more)
not provided
GUncertain significance