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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYNCRIP
(D16G)
Single nucleotide variant
(missense variant +1 more)
See cases
GUncertain significance
SYNCRIP
(G135fs +2 more)
Microsatellite
(frameshift variant)
not provided
GLikely pathogenic
SYNCRIP
(A369T +3 more)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
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