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Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130062628, TNFRSF11A
Single nucleotide variant
(5 prime UTR variant)
Bone Paget disease
+3 more
GBenign/Likely benign
LOC130062628, TNFRSF11A
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
TNFRSF11A
Single nucleotide variant
(intron variant)
Bone Paget disease
+3 more
GBenign/Likely benign
TNFRSF11A
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
TNFRSF11A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TNFRSF11A
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
TNFRSF11A
(R129C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TNFRSF11A
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TNFRSF11A
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
TNFRSF11A
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
TNFRSF11A
(V209I +1 more)
Single nucleotide variant
(missense variant +1 more)
Paget disease of bone 2, early-onset
+3 more
GBenign
TNFRSF11A
(K240E +1 more)
Single nucleotide variant
(missense variant +1 more)
TNFRSF11A-related condition
+6 more
GConflicting classifications of pathogenicity
TNFRSF11A
(E346G +1 more)
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
TNFRSF11A
Single nucleotide variant
(synonymous variant +1 more)
TNFRSF11A-related condition
+3 more
GConflicting classifications of pathogenicity
TNFRSF11A
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
TNFRSF11A
(T447I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
TNFRSF11A
Single nucleotide variant
(synonymous variant +1 more)
TNFRSF11A-related condition
+1 more
GConflicting classifications of pathogenicity
TNFRSF11A
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
TNFRSF11A
(S529G +3 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
TNFRSF11A
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+1 more
GBenign
TNFRSF11A
(M566L +3 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+1 more
GUncertain significance
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