U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 27

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANTXR1
(R190fs)
Deletion
(frameshift variant)
GAPO syndrome
GLikely pathogenic
ANTXR1
Single nucleotide variant
(splice donor variant)
GAPO syndrome
GLikely pathogenic
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
ANTXR1
Deletion
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Insertion
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
Single nucleotide variant
(intron variant)
GAPO syndrome
+1 more
GBenign
ANTXR1
(G369S)
Single nucleotide variant
(missense variant)
GAPO syndrome
GUncertain significance
ANTXR1
(G27V)
Single nucleotide variant
(missense variant)
GAPO syndrome
GUncertain significance
ANTXR1
Single nucleotide variant
(intron variant)
Capillary infantile hemangioma
+3 more
GBenign
ANTXR1
(G384S)
Single nucleotide variant
(missense variant)
GAPO syndrome
GLikely pathogenic
ANTXR1
Single nucleotide variant
(synonymous variant)
GAPO syndrome
GLikely pathogenic
ANTXR1
(A408fs)
Duplication
(frameshift variant)
GAPO syndrome
GLikely pathogenic
ANTXR1
Single nucleotide variant
(intron variant)
ANTXR1-related condition
GUncertain significance
ANTXR1
(R88*)
Single nucleotide variant
(nonsense)
GAPO syndrome
GPathogenic
ANTXR1
(R169*)
Single nucleotide variant
(nonsense)
GAPO syndrome
GLikely pathogenic
Format
Items per page
Sort by
Choose Destination