Variants in gene GRIN2A with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met)	rs145956175	0.00105
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser)	rs77029288	0.00068
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly)	rs145063086	0.00067
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=)	rs77705198	0.00059
NM_001134407.3(GRIN2A):c.1410T>G (p.Thr470=)	rs372058698	0.00028
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=)	rs372083517	0.00022
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg)	rs183029507	0.00007
NM_001134407.3(GRIN2A):c.2966A>G (p.Asn989Ser)	rs531782747	0.00005
NM_001134407.3(GRIN2A):c.3427G>A (p.Glu1143Lys)	rs61758996	0.00004
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile)	rs587780353	0.00004

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