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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCNT
Single nucleotide variant
(splice donor variant)
Microcephalic osteodysplastic primordial dwarfism type II
GLikely benign
PCNT
Single nucleotide variant
(splice acceptor variant)
Microcephalic osteodysplastic primordial dwarfism type II
GLikely pathogenic
PCNT
(E1106* +1 more)
Duplication
(nonsense)
Microcephalic osteodysplastic primordial dwarfism type II
GLikely pathogenic
PCNT
(Q1568fs +1 more)
Duplication
(frameshift variant)
Microcephalic osteodysplastic primordial dwarfism type II
GLikely pathogenic
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