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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HOXD13
(A14V)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
HOXD13
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
HOXD13
Deletion
(inframe_deletion)
not provided
+1 more
GBenign/Likely benign
HOXD13
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign
HOXD13
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
HOXD13
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
HOXD13
(R274*)
Single nucleotide variant
(nonsense)
Synpolydactyly
+13 more
GPathogenic/Likely pathogenic
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