U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 1 to 100 of 3534

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCA10, ADAM11
+2032 more
Copy number gain
See cases
GPathogenic
LOC130060795, LOC130060796
+1753 more
Copy number gain
See cases
GPathogenic
APOH, AXIN2
+109 more
Copy number loss
See cases
GPathogenic
AXIN2, GNA13
+16 more
Duplication
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2, LOC129390913
Deletion
Oligodontia-cancer predisposition syndrome
GLikely pathogenic
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Duplication
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Deletion
(3 prime UTR variant)
not provided
GLikely benign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
+1 more
GConflicting classifications of pathogenicity
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GBenign
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2, LOC129390913
Duplication
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(3 prime UTR variant)
not specified
GLikely benign
AXIN2
Single nucleotide variant
(stop lost)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
+1 more
GLikely benign
AXIN2
(D778V +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(D778Y +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
AXIN2
(D843N +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+3 more
GUncertain significance
AXIN2
(D843H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
(I777M +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
AXIN2
Duplication
(inframe_insertion)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(R776P +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(R841Q +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+2 more
GUncertain significance
AXIN2
(R776G +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
(R841W +1 more)
Single nucleotide variant
(missense variant)
AXIN2-related condition
+4 more
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(E775D +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(E775G +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
(G772fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
AXIN2
(G772S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
+2 more
GConflicting classifications of pathogenicity
AXIN2
(I770V +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(R769Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
AXIN2
(R834G +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
(R834W +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign/Likely benign
AXIN2
(G833D +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
(Y766C +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(M765I +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(M765I +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(M765R +1 more)
Single nucleotide variant
(missense variant)
Colorectal cancer
GUncertain significance
AXIN2
(M830T +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
AXIN2
(M830K +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
(M765V +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing 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
+2 more
GConflicting classifications of pathogenicity
AXIN2
(P829L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(V762A +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(V762M +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
+1 more
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
AXIN2-related condition
+4 more
GLikely benign
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
+1 more
GLikely benign
AXIN2
(T826K +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(T826M +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
AXIN2
(E825D +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
AXIN2
(E760K +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(D759E +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
AXIN2
(D824E +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
AXIN2
(D824V +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
(D759N +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
AXIN2
(E823fs +1 more)
Deletion
(frameshift variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Oligodontia-cancer predisposition syndrome
GLikely benign
AXIN2
(W757* +1 more)
Single nucleotide variant
(nonsense)
Oligodontia-cancer predisposition syndrome
GPathogenic
AXIN2
(W757R +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
AXIN2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
AXIN2
(I756T +1 more)
Single nucleotide variant
(missense variant)
Oligodontia-cancer predisposition syndrome
GUncertain significance
Format
Items per page
Sort by
Choose Destination