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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.1643G>A (p.Arg548Gln)	rs1554770044
NM_007327.4(GRIN1):c.1910C>T (p.Ala637Val)	rs1554770221
NM_007327.4(GRIN1):c.1974C>G (p.Asp658Glu)	rs1064795712
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu)	rs1328780843
NM_007327.4(GRIN1):c.2417C>T (p.Ala806Val)	rs1554770589
NM_007327.4(GRIN1):c.2444G>A (p.Gly815Glu)	rs1833698535
NM_007327.4(GRIN1):c.2500G>C (p.Glu834Gln)	rs1588735834
NM_007327.4(GRIN1):c.421G>A (p.Val141Met)	rs1293947350
NM_007327.4(GRIN1):c.448G>A (p.Val150Met)	rs1187375556

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