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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCF3
(S635* +2 more)
Single nucleotide variant
(nonsense)
Agammaglobulinemia 8, autosomal dominant
GPathogenic
TCF3
Deletion
Agammaglobulinemia 8b, autosomal recessive
GPathogenic
TCF3
Single nucleotide variant
(intron variant)
Agammaglobulinemia 8, autosomal dominant
GUncertain significance
TCF3
(A43V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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