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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TIMELESS
(R1080*)
Single nucleotide variant
(nonsense +1 more)
Advanced sleep phase syndrome, familial, 4
GPathogenic
FBXL3
(C358R)
Single nucleotide variant
(missense variant)
Intellectual disability, short stature, facial anomalies, and joint dislocations
GPathogenic