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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPHB2
(G1017fs)
Duplication
(3 prime UTR variant +1 more)
Bleeding disorder, platelet-type, 22
GUncertain significance
EPHB2, MIR4253
(D315E)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
EPHB2
Copy number gain
See cases
GBenign
EPHB2
(G786R +2 more)
Single nucleotide variant
(missense variant)
Neoplasm of the large intestine
GLikely pathogenic
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