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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERBB3
(A1337T)
Single nucleotide variant
(missense variant)
Erythroleukemia, familial, susceptibility to
+1 more
GConflicting classifications of pathogenicity
NF2
(F62S)
Single nucleotide variant
(missense variant +2 more)
Neurofibromatosis, type 2
GUncertain significance