Variants in gene GRIN2A with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.1492G>A (p.Gly498Ser)	rs757713617
NM_001134407.3(GRIN2A):c.2042G>A (p.Arg681Gln)	rs753203288
NM_001134407.3(GRIN2A):c.2138T>G (p.Val713Gly)	rs1057518070
NM_001134407.3(GRIN2A):c.2197G>A (p.Ala733Thr)	rs796052550
NM_001134407.3(GRIN2A):c.2452G>A (p.Ala818Thr)	rs1555483699
Single allele

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