List of variants in gene GRIN2A reported as uncertain significance by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.869C>T (p.Ala290Val)	rs199528312	0.00001
NM_001134407.3(GRIN2A):c.250A>T (p.Thr84Ser)	rs1006328489
NM_001134407.3(GRIN2A):c.3032G>T (p.Arg1011Leu)	rs1163766811
NM_001134407.3(GRIN2A):c.3339_3342del (p.Arg1114fs)	rs1379582796
NM_001134407.3(GRIN2A):c.3712G>A (p.Ala1238Thr)	rs2141129928

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