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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.394-4G>A	rs202180269	0.00009
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.1904T>G (p.Val635Gly)	rs2538640589
NM_007327.4(GRIN1):c.1975C>G (p.Arg659Gly)
NM_007327.4(GRIN1):c.734A>T (p.Tyr245Phe)	rs893141433

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