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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPRED1
Single nucleotide variant
(intron variant)
not specified
GBenign
SPRED1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign
SPRED1
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
SPRED1
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
SPRED1
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
SPRED1
(I234M)
Single nucleotide variant
(missense variant)
Legius syndrome
+2 more
GConflicting classifications of pathogenicity
SPRED1
(Q339*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
SPRED1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign
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