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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
+1 more
GLikely benign
AXIN2
(H747Y +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GConflicting classifications of pathogenicity
AXIN2
(P740S +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GUncertain significance
AXIN2
(C551R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+5 more
GUncertain significance
AXIN2
(Q188R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+3 more
GConflicting classifications of pathogenicity
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