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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM53B, FAM53B-AS1
(R12Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
FAM53B, FAM53B-AS1
(R12W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance