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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC109611589, RUNX2
Deletion
(inframe_deletion)
not specified
GLikely benign
LOC109611589, RUNX2
(Q51K +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
LOC109611589, RUNX2
Microsatellite
(inframe_deletion)
not specified
+1 more
GConflicting classifications of pathogenicity
LOC109611589, RUNX2
Microsatellite
(inframe_deletion)
Cleidocranial dysostosis
+2 more
GBenign/Likely benign
LOC109611589, RUNX2
Single nucleotide variant
(synonymous variant)
Cleidocranial dysostosis
+2 more
GBenign
RUNX2
(N177K +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
RUNX2
(R225Q +1 more)
Single nucleotide variant
(missense variant)
RUNX2-related condition
+3 more
GPathogenic
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