Variants in gene GRIN1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.1643G>A (p.Arg548Gln)	rs1554770044
NM_007327.4(GRIN1):c.1858G>A (p.Gly620Arg)	rs797045047
NM_007327.4(GRIN1):c.1858G>C (p.Gly620Arg)	rs797045047
NM_007327.4(GRIN1):c.1913G>C (p.Gly638Ala)	rs1393555703
NM_007327.4(GRIN1):c.1921A>G (p.Met641Val)	rs2131299136
NM_007327.4(GRIN1):c.2381G>A (p.Arg794Gln)	rs781053477
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys)	rs1554770667

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