ClinVar Miner

List of variants in gene GRIN1 reported as uncertain significance for Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser) rs148008303 0.00003
NM_007327.4(GRIN1):c.1851C>A (p.Ser617=) rs555866770
NM_007327.4(GRIN1):c.1864+20G>C rs1833616244

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