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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPG2
(L3571F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HSPG2
(N3369K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HSPG2
(G3324R +1 more)
Single nucleotide variant
(missense variant)
Schwartz-Jampel syndrome
+3 more
GLikely pathogenic
HSPG2
(T934fs +1 more)
Duplication
(frameshift variant)
not provided
GLikely pathogenic
HSPG2
(A680T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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