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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYNC1I2
Single nucleotide variant
(intron variant)
Neurodevelopmental disorder with microcephaly and structural brain anomalies
GUncertain significance
DYNC1I2
(C88G)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with microcephaly and structural brain anomalies
GUncertain significance
DYNC1I2
Single nucleotide variant
(splice acceptor variant)
Neurodevelopmental disorder with microcephaly and structural brain anomalies
GLikely pathogenic
DYNC1I2
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
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