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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNB, LOC129936935
Single nucleotide variant
(synonymous variant)
FLNB-Related Spectrum Disorders
+3 more
GBenign/Likely benign
FLNB, LOC129936935
Single nucleotide variant
(synonymous variant)
Spondylocarpotarsal synostosis syndrome
+7 more
GBenign/Likely benign