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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXIN2
(A603P)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
+4 more
GBenign/Likely benign
AXIN2
(A591V)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
AXIN2
(S390G)
Single nucleotide variant
(missense variant)
AXIN2-related condition
+4 more
GConflicting classifications of pathogenicity
AXIN2
(S244L)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GUncertain significance
AXIN2
(A208V)
Single nucleotide variant
(missense variant)
AXIN2-related condition
+4 more
GConflicting classifications of pathogenicity
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