ClinVar Miner

List of variants in gene DYNC1I2 reported as uncertain significance for Neurodevelopmental disorder with microcephaly and structural brain anomalies

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378.3(DYNC1I2):c.1546C>A (p.Pro516Thr)	rs767705533
NM_001378.3(DYNC1I2):c.1678-3T>C
NM_001378.3(DYNC1I2):c.245-19T>G

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