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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSPP
(R66K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DSPP
(R68W)
Single nucleotide variant
(missense variant)
DSPP-related condition
+3 more
GBenign
DSPP
(T72A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DSPP
(D243N)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
DSPP
(R354C)
Single nucleotide variant
(missense variant)
Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1
+2 more
GConflicting classifications of pathogenicity
DSPP
(V355I)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
DSPP
(R358K)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
DSPP
(S1220R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
DSPP
Single nucleotide variant
Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1
+5 more
GBenign
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