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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SGSH
(R456H)
Single nucleotide variant
(missense variant +2 more)
not provided
+2 more
GBenign
SGSH
(V387M)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GBenign/Likely benign
SGSH
(V361I)
Single nucleotide variant
(missense variant +2 more)
Mucopolysaccharidosis, MPS-III-A
+2 more
GBenign
SGSH
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
SGSH
Single nucleotide variant
(synonymous variant +1 more)
SGSH-related disorder
+2 more
GConflicting classifications of pathogenicity
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