List of variants in gene GRIN1 reported as uncertain significance for Intellectual disability, autosomal dominant 8; Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive; Developmental and epileptic encephalopathy 101

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.957G>A (p.Pro319=)	rs766888803	0.00001
NM_007327.4(GRIN1):c.1387C>T (p.Leu463Phe)
NM_007327.4(GRIN1):c.1975C>G (p.Arg659Gly)
NM_007327.4(GRIN1):c.734A>T (p.Tyr245Phe)	rs893141433

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