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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PON3
Duplication
(3 prime UTR variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
(A179D)
Single nucleotide variant
(missense variant)
not provided
GBenign
PON3
(V166M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(synonymous variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
(R32*)
Single nucleotide variant
(nonsense)
not specified
+2 more
GConflicting classifications of pathogenicity
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Deletion
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(intron variant)
not provided
GBenign
PON3
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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