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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMR1
(K119N)
Single nucleotide variant
(missense variant +1 more)
Fragile X syndrome
GLikely benign
FMR1
Single nucleotide variant
(3 prime UTR variant +1 more)
Fragile X syndrome
GBenign