List of variants in gene GRIN1 reported as pathogenic for not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.1643G>A (p.Arg548Gln)	rs1554770044
NM_007327.4(GRIN1):c.1658C>T (p.Ser553Leu)	rs2131297379
NM_007327.4(GRIN1):c.1670C>G (p.Pro557Arg)	rs878853143
NM_007327.4(GRIN1):c.1850C>G (p.Ser617Cys)
NM_007327.4(GRIN1):c.1852G>A (p.Gly618Ser)	rs1833614590
NM_007327.4(GRIN1):c.1858G>C (p.Gly620Arg)	rs797045047
NM_007327.4(GRIN1):c.1930G>A (p.Val644Met)	rs1554770248
NM_007327.4(GRIN1):c.1949A>T (p.Asn650Ile)	rs1131691590
NM_007327.4(GRIN1):c.1955C>T (p.Ala652Val)	rs1064797027
NM_007327.4(GRIN1):c.1975C>T (p.Arg659Trp)	rs1064797355
NM_007327.4(GRIN1):c.2414C>T (p.Pro805Leu)	rs1588735247
NM_007327.4(GRIN1):c.2443G>T (p.Gly815Trp)	rs797044925
NM_007327.4(GRIN1):c.2479G>A (p.Gly827Arg)	rs1451230055
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys)	rs1554770667

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