U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNFRSF11B
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
TNFRSF11B
(Q243H)
Single nucleotide variant
(missense variant)
Hyperphosphatasemia with bone disease
+1 more
GUncertain significance
TNFRSF11B
(C145G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TNFRSF11B
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
TNFRSF11B
(C107W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TNFRSF11B
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
TNFRSF11B
Single nucleotide variant
(synonymous variant)
Hyperphosphatasemia with bone disease
+1 more
GConflicting classifications of pathogenicity
TNFRSF11B
(L50I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TNFRSF11B
Single nucleotide variant
(synonymous variant)
Hyperphosphatasemia with bone disease
+1 more
GConflicting classifications of pathogenicity
TNFRSF11B
Single nucleotide variant
(synonymous variant)
TNFRSF11B-related condition
+1 more
GConflicting classifications of pathogenicity
TNFRSF11B
(N3K)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
Format
Items per page
Sort by
Choose Destination