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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP53
(K292I +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
KCNQ1OT1
Deletion
Beckwith-Wiedemann syndrome
GPathogenic