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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PROS1
(V527fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
PROS1
(C120fs +1 more)
Duplication
(frameshift variant)
not provided
GLikely pathogenic
PROS1
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
PROS1
(T78M +1 more)
Single nucleotide variant
(missense variant)
Protein S deficiency disease
+4 more
GConflicting classifications of pathogenicity
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