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Links from MedGen

Items: 1 to 100 of 2981

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AXIN2
(T246I)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(G214V)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(S616W)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E611G)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(R834G +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(W757R +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(D440E)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S390C)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(K503E)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(T437R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(A368S)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(F17Y)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S84P)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P670R +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(T254I)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(V248I)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E100K)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(A343T)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(Y135H)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(Y138H)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(I144T)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(Q509R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(Y550H)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E415D)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(V327M)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S3N)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(Y196C)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(I531fs)
Deletion
(frameshift variant)
Oligodontia-cancer predisposition syndrome
GPathogenic
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(S73F)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P450A)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(V524F)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E746D +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(E233del)
Microsatellite
(inframe_deletion)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(A131G)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P462L)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S193T)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(Q89K)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(I285M)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P609T)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(P13L)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P593L)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(L215F)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(Q332R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Duplication
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P293S)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(C222S)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(intron variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(D778V +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Duplication
(inframe_insertion)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Indel
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(G270E)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E587*)
Single nucleotide variant
(nonsense +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(M362V)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(M210K)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(G67R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E392D)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(A492S)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant +1 more)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(Q164R)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(D106G)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(P579H)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(Q607R)
Single nucleotide variant
(missense variant +1 more)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(M565I)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(S466fs)
Deletion
(frameshift variant)
Oligodontia-cancer predisposition syndrome
GPathogenic
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(P618T +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
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